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All are aware of the protection of personal data

Illustration : European data privacy day - RGPD

Table of Contents

Saturday, January 28th, 2023, will be Data Privacy Day. Created in 2006 by the European Council, it aims to make users aware of the importance of protecting their personal data. For companies, it’s an opportunity to ensure that they are compliant with the law.

What is personal data ?

Personal data is all the information that identifies a person. A person can be identified in several ways:

  • Directly (name, first name)
  • Indirectly (examples: customer number, phone number, photo,…)
  • From a single data (examples: social security number, DNA)
  • From the crossing of several data (example: date of birth + address)

Article 4 of the GDPR defines personal data as follows:

“any information relating to an identified or identifiable natural person (‘data subject’); an identifiable natural person is one who can be identified, directly or indirectly, in particular by reference to an identifier such as a name, an identification number, location data, an online identifier or to one or more factors specific to the physical, physiological, genetic, mental, economic, cultural or social identity of that natural person.”

Personal data vs. sensitive data

Often confused, sensitive data is a particular category of personal data. Sensitive data is particularly at risk and benefits from a reinforced legal protection regime. The GDPR prohibits the processing of sensitive data.

Article 9 of the GDPR defines sensitive data as revealing:

  • Racial or ethnic origin,
  • Political opinions,
  • Religious or philosophical beliefs,
  • Trade union membership,
  • The processing of genetic data, biometric data for the purpose of uniquely identifying a natural person,
  • Data concerning health,
  • Data concerning a natural person’s sex life or sexual orientation.

What is the GDPR ?

The General Data Protection Regulation frames personal data processing on the European Union’s territory. Entered into force on May 25th, 2018, it harmonizes European rules. Its objective is twofold:

  • To protect and facilitate the rights of users
  • To make organizations that process personal data accountable.

Who is concerned about the GDPR ?

Any organization can be concerned, whatever its size, country of establishment, and activity. Indeed, the RGPD applies to any organization, public or private:

  • Established on the territory of the European Union,
  • Or that its activity directly targets European residents.

Non-European companies have the same obligations as long as they offer products or services to European residents.

Regulatory bodies

In France, the CNIL is the administrative authority enforcing the GDPR. Its European counterpart is the European Data Protection Committee (EDPS).

Roles of the CNIL

  • Inform individuals and professionals, and protect individual liberties,
  • To assist organizations in their compliance with the GDPR,
  • Anticipate the ethical challenges of data and innovate: the CNIL, alongside companies, participates in research in the field of privacy and personal data,
  • Controlling organizations.

Best pratices to comply with the GDRP

If personal data is not the core of your business, being compliant with the RGPD is quite simple. To do so, follow these best practices.
Source CNIL

Collect only the necessary data
The data you keep must be strictly necessary for your business. Do not collect any "sensitive" data. If it is not the case, it is the occasion to sort out your data!
Be transparent
Individuals must consent to the use of their data to use it. Therefore, it requires that they are clearly informed about the collection and use of their data. The GDPR requires that consent be "free, specific, informed, and unambiguous." The "default" consent is, therefore, not tolerated.
Make it easy for people to exercise their rights
Individuals (customers, service providers, employees, etc.) must retain control over the data that concerns them. Therefore, organize modalities allowing people to exercise their rights and respond as soon as possible to these requests. For subscribers to your email list, for example, provide an easily accessible unsubscribe and update form.
Set retention periods
You can't keep data indefinitely. You need to define the life cycle of the data. In most cases, there is no set rule for how long data should be kept. It is up to the company to define a relevant duration.
Secure data and identify risks
Server security should be a priority. Limit access and manage wifi networks; Use secure passwords; Perform regular updates and backups; Secure your websites; Secure your archives. Protect your data by replicating it. A recovery plan is required in the event of data loss. Ensure data confidentiality and integrity by encrypting data.

Control ans sanctions of the CNIL

The CNIL can check the proper compliance with the law with companies that process personal data.

  • Warning and Call to Order: This is not a sanction but a corrective measure.
  • An injunction under penalty: This is an order to comply with a sum to be paid in the event of non-compliance with the decision.
  • Sanction: A fine of up to 20 million euros or, for a company, up to 4% of worldwide turnover.

GAFAMs are not spared. In January 2022, the CNIL sanctioned GOOGLE with a 150 million euro fine and FACEBOOK with a 60 million fine for non-compliance with the cookie management rules. Indeed, their procedures do not allow users to refuse cookies as easily as to accept them.

Data security at GxpManager

The security of your data is part of the GxpManager platform’s DNA.

  • Our sovereign data center is located in France. We have chosen a European host to avoid exposing our clients to the legal and financial risks inherent to American companies, particularly those subject to extra-territorial laws such as the Cloud Act.
  • Updates, backups, restorations, and archiving are automated.
  • Your data is accessible online 24 hours a day.
  • A data encryption system ensures the integrity of your data.
  • Availability of your data: Provision of a disaster recovery plan (DRP) with very high availability and three redundant servers.

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The quality management system represents a challenge for companies. When it is digitalized, it becomes an undeniable performance driver.

Visual representing a laptop computer with virtual screens representing stylized sheets of paper

Table of Contents

Quality is essential in all fields, and ensuring that quality standards are respected is a priority for everyone at all levels of the product or service life cycle. Therefore, the digitization of quality management systems (QMS) is nowadays inevitable, especially in regulated sectors.

What is Quality Management System Software (QMS)?

Quality management System software is a tool that enables an organization to effectively manage its quality management activities and comply with applicable quality regulations and standards.

It allows a company to plan, implement, monitor, and control its quality management activities. In addition, quality management software can automate and manage various quality management system tasks, such as data collection, analysis, non-conformance management, and stakeholder communication.

QMS software can also help ensure that the company complies with applicable regulations and quality standards and can provide reports and analysis to track progress and identify areas for improvement.

Why implement a digital quality management system?

There are several reasons why (highly regulated) industries may want to implement a digitalized Quality Management System:

  • Product and service quality improvement: a digitalized quality management system can help companies improve the quality of their products and services by identifying and correcting quality issues more quickly and efficiently.
  • Regulatory compliance: In highly regulated industries, it is critical to comply with applicable regulations. A digital quality management system can help companies comply with regulatory requirements by keeping track of all company activities and ensuring that products and services meet required standards.
  • Improved operational efficiency: a digital quality management system can help companies improve operational efficiency by automating specific tasks and enabling better collaboration and communication.
  • Improved corporate reputation: by improving the quality of its products and services and complying with regulations, a company can improve its reputation with its customers and stakeholders.

    A digitalized quality management system can help companies improve the quality of their products and services, comply with regulations, improve operational efficiency and enhance their reputation.

What are the potential barriers to implementing a quality management system?

Implementing a quality management system is a process with limitations that can be overcome with the right solution.

Pain pointsSolutions
Cost
Implementing and maintaining a quality management system can be expensive, especially for small businesses.One solution does not fit all! Quality management software is designed according to the size of the company and its needs. Therefore, avoid "generic" solutions.
Time
Implementing and maintaining a quality management system can be time-consuming, especially if the company has to adapt to new regulations or quality standards.In all cases, the company must adapt to new regulations. Quality management software integrates the updates when necessary. Software that is already compliant facilitates the evolution in terms of time and resources (gain).
Complexity
A quality management system can be complex, especially if the company has many stakeholders and must follow many different regulations and quality standards.Implementing a quality management system must be collegial with all stakeholders to decomplex it. Thus, all key users have visibility in the implementation/modeling of the management platform.
Lack of flexibility
A quality management system can be rigid and inflexible, making it difficult to adapt to changes in the business environment.The choice of the quality management platform must be made with a vision of the company's evolution. QMS applications evolve with the company and its progressing needs.
Lack of employee engagement
If employees are not committed to the quality management system, it can be challenging to maintain its effectiveness.When selecting and implementing the QMS, key users must be an integral part of the process so that all understand the system’s benefits and participate in its improvement.
Weakness of the technology used
If the technology used to implement the quality management system is outdated or unreliable, it can affect the quality of the data collected and the company's ability to make informed decisions.When choosing the technology used for quality management, the platform’s evolution must be a criterion of choice so that the system grows with the company.

Towards a digitalized Quality Management Solution

One of the main reasons to digitize the quality management system is to comply with the regulations in place, as paper forms or Excel spreadsheets are becoming security and data integrity problems. There are several advantages to digitizing your quality management system (QMS) for better compliance with regulations:

 

  • Improved traceability: by using QMS software or applications, it is possible to keep track of all company activities and generate reports that can be used to demonstrate regulatory compliance.
  • Accurate and reliable data: Using quality management software, data can be collected and stored accurately and reliably, which can help demonstrate regulatory compliance.
  • Easy to update: Quality management software makes it easy to update processes and procedures when regulations or quality standards are updated.
  • Improved operational efficiency: By using quality management software, tasks can be automated and time saved, improving operational efficiency.
  • Simplified audit management: Internal and external audit management is simplified, saving time in reviewing data and documents. Centralization of audit activities and follow-up of corrective and preventive actions.

Digitizing its QMS can help a company improve its activities’ traceability, ensure data accuracy and reliability, easily update its processes and procedures in case of regulatory changes, and improve its operational efficiency, especially during internal or external audits.

Implementing a new quality management system or improvement through digitalization is a strategic issue for all companies that depends on several factors: the company’s size, the complexity of the processes in place in the different departments, and the company’s long-term vision.

In all cases, data integrity, compliance, and resource savings (time, cost, and human) are competitive advantages that companies must have today. Quality management system digitalization solutions are available, have a look at QMS-4-SME.

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Uncategorized

On November 29th and 30th, 2022, the 18th edition of the international business meetings of the Pharmaceutical, Chemical, and Petrochemical industries happened at the Espace Tête d’Or in Lyon.

PCH Meetings Lyon 2022

Elisabeth and Marc welcomed the numerous actors from these different industries. Many exchanges took place on the industrial and digital evolutions and on the opportunities offered to GxpManager, which is at the heart of these digital transformations.

Elisabeth and Marc welcomed the numerous actors from these different industries. Many exchanges took place on the industrial and digital evolutions and on the opportunities offered to GxpManager, which is at the heart of these digital transformations.

The forum included conferences led by experts on market news, innovations, and feedback from manufacturers.

Jérôme Tomaselli, President of GxpManager, presented “the advantages of digitalization in a regulated environment” to an audience of professionals. He received positive feedback and confirmation of the increasing demand for digitalized and compliant solutions.

PCH Meetings Lyon 2022
Marc’s word
« The approach proposed by PCH Meetings is particularly relevant for GxpManager: qualitative and efficient meetings as they are well targeted and “timed”. Our solutions presented seduced both the visitors and the exhibitors of the show. »
A word from Elisabeth
« The meetings were enriching, and the GxpManager solutions won over the public. Prospects are undertaking more and more digitalization projects in their companies to make their quality system more harmonized and, most of all, compliant with regulatory authorities. »

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Thursday, November 17th, the A3P forum was held in Belgium. Our sales team was present.

A3P Belgium Forum - Digitalization or digitization

Since 1986, the A3P association has been a significant player in the pharmaceutical and biotechnology industry. The association contributes to the development of the production of clean and sterile drugs and products through international events where its members share their technical, scientific, and regulatory experiences.

The theme of the A3P Belgium forum on Thursday was “Digitalization or digitization: from process development to GMP (Good Manufacturing Practice) facility design.” This event is punctuated by conferences on regulatory aspects and validation concerns. The forum concluded with an interesting visit to the CDMO site of Mithra Pharmaceuticals in Flémalle. The guide was none other than the site director, Mr. Renaat Baes.

An atypical place

The exhibition took place in the castle of Val Saint Lambert, a high position in the Belgian crystal industry. This site is known for its castle, abbey, museum, and of course, its crystal factory still in activity.

Visual of Chateau du Val Saint Lambert - A3P Belgium - Digitalization or digitization

According to the GxpManager team, this unusual place was a pleasant surprise. Moreover, our Belgian friends were warm and welcoming, as usual. Furthermore, the organization was also a good surprise since the animators gave them a good orientation on the day’s program and respected the timing in an academic and relaxed atmosphere.

Elisabeth’s plus:

“What I liked best were the moments of exchange with the participants. Especially during the meal on large tables. It was pleasant to exchange with professionals! “The visit of the Mithra factory was also very well organized. The factory was particularly functional and well thought out. In conclusion, the experience was enriching.”

Several persons from the company welcomed the participants and explained their missions and the implemented processes.

Many companies were present at this forum, such as Baxter, Takeda, GSK, and several biotechs. This forum allowed us to develop interesting contact with other exhibitors, with good promises of partnership.

Marc’s extra : 

“We had lunch with one of our major customers who gave us a glimpse of new opportunities for collaboration on other topics. GxpManager put a smile on their face as they concluded by telling us, “You are the best news of the day!” “

The A3P Belgium forum has shown a significant evolution in the Pharma sector with digitization and industrialization 4.0. With a growing acceptance of digitization in this sector, especially for paper forms and Excel, and despite the well-known barriers to change.

The A3P forum brought our staff new knowledge and interesting contacts in the Life Sciences community. On the other hand, even though the GxpManager team traveled to Belgium, they did not bring any waffles (from Liege) for the rest of the team. But they promise to come back next year!

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Uncategorized

An essentiel and rewarding visit

GxpManager at ILMAC exhibition on Wednesday September 28, 2022

ILMAC LAUSANNE has been the platform for the chemical and life sciences industry in Switzerland and Europe since 1959. The exhibition is dedicated to the users of these sectors and presents all industrial applications in process and laboratory technology. It is aimed at specialists in the pharmaceutical, chemical, biotechnology, food, beverage, cosmetics and other regulated industries. This year, it brought together 150 exhibitors and welcomed more than 1800 visitors.

Elisabeth and Marc visited the ILMAC exhibition on Wednesday September 28, 2022, to meet the actors of the chemical and life sciences industries present in Switzerland and Europe. They presented GxpManager‘s Low code No code platform and its digital transformation applications which are essential today.

Indeed, the digitalization of technological processes is at the heart of the digital transformation of companies in regulated industries, with the automation of processes, continuous and self-calibrating production, dematerialization of Excel tables and other master data or forms . All technological processes nowadays integrate the digitization of data with validation and qualification requests in order to comply with the regulations in place.

 

Marc, GxpManager’s Sales and Marketing Manager, went to meet the exhibitors in Lausanne:

“We had the pleasure to exchange on the needs, the market’ state and the upcoming developments in the world of laboratory equipment manufacturers, mainly. The diversity, in terms of size and language, of the exhibitors allowed us to meet actors of the Life Sciences world that we don’t always see on French trade-shows. And once again, we appreciated the welcome and dynamism of our Swiss contacts.”

 

Marc was accompanied by Elisabeth, Business Developer :

“My first exhibition with GxpManager! I had some good exchanges with players in the Life-Sciences world. This allowed me to present GxpManager and its solutions, such as the dematerialization of forms, the digitization of Excel spreadsheets or our QMS-4-SME solution , which is a Quality Management System, which aroused a lot of interest among the exhibitors.”

 

Elisabeth has been with GxpManager since the beginning of 2022, and as a Business Developer she will be attending many trade shows and events to propose and present all the critical data digitization solutions, Low code No code (LCNC), available on the GxpManager platform.

Next year, GxpManager might be present as an exhibitor at the ILMAC exhibition in order to propose to the visitors solutions of digitization of critical data, and to meet new partners and already known one, as GxpManager has been working with large pharmaceutical accounts in Switzerland for many years.

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Article by Patrick RENARD published on DeviceMed.

Digitization of data: from “GreenIT” to “Data integrity”

Expert en traitement des données critiques, GxpManager nous livre ici sa vision de la digitalisation qu’il articule autour de sa plateforme logicielle éponyme. Dotée d’un générateur d’applications, celle-ci garantit la conformité aux exigences réglementaires, comme il se doit dans le monde du DM.

La qualité a une longue histoire. Il y a plus de 2000 ans, Vitruve décrivait déjà les techniques romaines afin de garantir à l’empire la construction d’ouvrages robustes, de façon homogène.

Autrefois, il fallait un long apprentissage pour qu’un artisan acquière les compétences nécessaires à la réalisation d’objets de qualité. Puis l’ère industrielle arriva, avec la segmentation des tâches et leur description précise dans des instructions de travail. On voulut ensuite s’assurer que les opérateurs suivaient réellement les instructions : les enregistrements qualité étaient nés.

Ainsi, la consommation de papier dans les entreprises s’envola ! A chaque exécution de tâche, son lot de papier, ce qui se traduisit par la déforestation. D’où le développement ces dernières années des concepts de « GreenIT » (ou Numérique responsable en français) et de « Paperless » (Dématérialisation) pour diminuer l’empreinte environnementale des industriels.

L’informatique était-elle prête pour la révolution écologique ?

Au début de l’informatique, chaque logiciel était élaboré sur mesure, ce qui générait des problèmes récurrents, issus du fait d’utilisateurs exprimant mal leurs besoins auprès d’informaticiens ne les assimilant pas correctement. Ces problèmes engendraient des retards, des surcoûts et des échecs, car modifier un logiciel spécifique est long, coûteux et générateur de difficultés techniques parfois insurmontables.

Les éditeurs ont alors proposé des progiciels répondant à des besoins prédéfinis auxquels les utilisateurs doivent se conformer. Mais cette spécialisation dans une activité particulière multiplie le nombre de logiciels dans l’entreprise, chacun étant doté de sa propre ergonomie, de ses propres évolutions et de ses interfaces spécifiques. Au final, la maintenance devient laborieuse et toute évolution difficile à suivre.

La plateforme GxpManager intègre, sous le nom de GxpMedicalDevices, un ensemble d’applications spécifiques aux dispositifs médicaux, prêtes à l’emploi. Celles-ci couvrent aussi bien le cycle de vie des produits, la validation que le système de management de la qualité.

Il existe des progiciels couvrant une multitude de besoins et de métiers, mais ils impliquent une implémentation longue et complexe réservée à des experts. L’entreprise devient alors dépendante et toute évolution se révèle vite sensible et coûteuse. La solution de contournement est trop souvent la « ShadowIT » (utilisation par les employés de logiciels sans accord du département informatique), ou le recours intensif à Excel. Cela redonne à l’utilisateur une agilité perdue mais il doit passer sous les radars des directions informatiques avec les risques d’erreurs notoires de manipulation des données que comporte un tableur.

Désormais, face également à la pression sociale et environnementale, les autorités réglementaires veulent à la fois réduire la quantité de papier utilisée et éradiquer les fichiers Excel que plus personne ne cautionne réellement du fait avéré de leur non-conformité et de l’absence d’audit trail (piste de contrôle), de gestion des versions, de signature électronique, de gestion d’accès…

Générer, sans programmation, des applications conformes

 

On aurait pu croire à l’impasse mais de nouvelles technologies émergent pour marier GreenIT et Data Integrity, que l’on peut traduire par la maîtrise des données critiques, essentielles à la conformité.

Le concept de Low Code, No Code fait partie de ces technologies. Il s’agit d’utiliser un générateur d’applications pour créer des logiciels sans programmation : c’est rapide, sans aucun bogue, agile et cela réduit les coûts de validation. Encore faut-il que les applications générées soient conformes aux exigences réglementaires. C’est le positionnement stratégique de la plateforme logicielle GxpManager qui génère nativement des applications avec audit trail, signature électronique, gestion des accès, etc.

Une organisation orientée « données »

 Jerôme Tomaselli, président de GXPManager

Jerôme Tomaselli, président de GXPManager

« Il est courant de confondre digitalisation et gestion électronique de documents », explique Jerôme Tomaselli, président de GxpManager. « Ranger des documents dans des placards électroniques ne fait que repousser le problème et immanquablement les données de ces documents ne seront pas exploitées. Cela fait tourner une armada de serveurs coûteux et polluants pour indexer les documents, mais ce n’est satisfaisant ni pour l’utilisateur, ni pour la Nature ».

Aujourd’hui, tout le monde s’accorde à dire que la richesse d’une entreprise réside dans ses données. « À l’analyse d’un document, il y a beaucoup de texte, mais peu de données pertinentes », ajoute M. Tomaselli. « L’exemple de la plateforme GxpManager est caractéristique de ce changement de paradigme, avec un point central qui n’est pas le document, mais la donnée elle-même. Qui a créé cette donnée ? Quand a-t-elle été créée ? Qui l’a modifiée? A quoi est-elle liée ? »

Avec cette approche, les utilisateurs approuvent les données à partir desquelles ils ont tout loisir de publier des documents.

L’autre avantage que GxpManager met en avant repose sur le fait que c’est l’unicité de cette donnée qui la rend exploitable : elle n’est plus noyée, multipliée dans des fichiers Excel ou des documents. « Elle est immédiatement disponible pour son exploitation », souligne M. Tomaselli. « C’est un trésor dont on peut ensuite tirer avantage en quelques clics : matrice de traçabilité instantanée, indicateurs de performance (KPI), analyses de tendances, tableaux de bord, rapports, etc. ».

Avec cette plateforme logicielle, GxpManager promet une digitalisation rapide des documents et des tableurs d’une entreprise, avec une interface simple, unique, sûre et intuitive. Mais la plateforme est conçue pour permettre aussi le développement d’applications sophistiquées qui vont s’intégrer naturellement avec la digitalisation des documents.

Pour accélérer encore la mise en œuvre d’un écosystème applicatif cohérent, GxpManager propose des applications standardisées qui répondent aux besoins classiques : gestion de la Qualité, des CAPA, des Audits, HSE…

« Les industriels ont là un outil précieux », conclut M. Tomaselli. « Facile d’utilisation, il répond aux préoccupations environnementales, réglementaires et de performance économique auxquelles ils font face ».

Lire l’article sur DeviceMe

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GxpManager innovates with its Low Code No Code solution.

During the program Le Grand Entretien by B Smart, Michel Denisot asked 5 questions to Jérôme Tomaselli about GXPManager on the challenges of digital transformation and the advantages of using GxpManager platform and applications.

What is your company offer and what is its goal?

GxpManager is a software editor since 2003 that offers a No Code Low Code solution in SaaS architecture. This solution is for companies that have to process critical data such as in the pharmaceutical sector. The goal is to develop applications without programming that meet all the requirements concerning the digitization of critical data in the company: electronic signature, audit trail, i.e. traceability of everything that is entered into the solution, access management, data traceability, workflow, secure storage of data and documents, validation of the infrastructure and the applications. Critical data is data that can be inspected at any time by customers, or regulatory or normative authorities, such as the ANSM in France, the FDA in the USA, for the health sector, to ensure the uniqueness and integrity of this data.

What are the challenges of digital transformation for you?

Quality systems require companies to describe all their critical activities in documents. To ensure that procedures are followed, operators must record critical data as they perform these activities. These records must be signed and approved. Currently, the vast majority of procedures and records are made on paper documents or Excel sheets. This represents a huge volume of paper! Today, regulatory authorities consider that processing critical data in these formats is no longer acceptable because the data integrity cannot be demonstrated. The challenge is to digitize thousands of forms – the basis of all quality and security systems in industry and services sectors such as banking, insurance, nuclear, chemical, health, etc… – and to have reliable, agile, fast and economical solutions.

What solutions do you offer to your customers?

We have three offerings. The first is à la carte” digitization of our customers’ paper forms (GxpForms) or Excel sheets (GxpXL). The development of the forms with GxpManager is carried out either by our teams or directly by the client, which allows him to reduce the cost of the project and to control all aspects. The second offer is digitization based on customizabled applications. We realize that, often, the same industry has similar needs, without being quite the same. So instead of starting from scratch, the customer uses an existing application and modifies it to fit his needs. Thanks to the No Code Low Code platform, this goes very fast. And finally the last one is the digitalization from standardized applications. For small structures, it can be interesting to use standard applications that have been developed and pre-validated. A simple training is enough to be operational to obtain a digitalized quality system. GxpManager’s application managers listen to customers’ needs and develop the applications regularly, which benefits all customers. All our offers are in SaaS architecture, i.e. in the Cloud and based on annual subscriptions per user.

What are the advantages of using your platform?

Thanks to our No Code Low Code platform, we can digitalize very quickly and reliably because the fact of not programming an application avoids all the classic problems of IT: design problems, poor expression of needs or bugs. The platform is SaaS, which means that the client does not need any infrastructure to use the GxpManager applications. It is therefore very simple and quick to implement. Customers regain agility. Thanks to the No Code Low Code platform, i.e. without any IT development, applications can be developed very quickly to adapt to changes in the company, customers, regulations, etc. Customers must demonstrate their compliance with regulatory or normative requirements in the event of customer or regulatory authority audits. GxpManager allows you to respond quickly and cost-effectively to the ever-increasing demands on data integrity. Last but not least, digitization with GxpManager saves thousands of trees every year by eliminating tons of paper.

What are your next short and long term goals?

The year 2021 has been dedicated to deploying our platform in the Life Sciences Industries: Pharma, Biotech and Medical Devices. We have won some very nice projects at Merck, Sanofi, Arkéma, Danone, GSK, Baxter. Leaders in the healthcare industry are choosing GxpManager as their digitalization platform. Our goal for 2022 is to implement our solution in all the subsidiaries of these major groups, all over the world, as it has proven its relevance in local projects. We have already started, since we are present in France, Switzerland, Belgium, China, Africa and the United States. We are also going to offer our platform to industries with a high demand for the digitization of critical data, such as Banking, Insurance, Energy and Transport, as well as the Services sector. In the medium term, we aim to become the world leader in the digitization of critical data.

 

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For implementing VPM and SVV management applications

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The pharmaceutical company Prophac represents pharmaceutical companies in Luxembourg in the field of human medicine, veterinary medicine and medical diagnosis. At the start of 2022, they decided to place their trust in the publisher GxpManager for a project targeting the implementation of VMP & SVV management applications. All the GxpManager teams are delighted with this new collaboration and are motivated to succeed in this project with the Prophac teams!

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LE GRAND ENTRETIEN

Jérôme Tomaselli, during the program Le Grand Entretien of February 24, 2022 on B-Smart, answers five questions asked by Michel Denisot...

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Best Wishes from GxpManager!

Heading for the 2022 Digital Transformation!
Together, let’s build a sustainable, responsible, united and more environmentally friendly future!
Always by your side to digitize your critical data, abandon paper, save trees
Best wishes from GxpManager!

Video and music credits
John Macdougall | Pixabay
Vector
www.bensound.com

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