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Skip to main content. Advice and reporting for the chemical and pharmaceutical industries. European Drug Regulatory Affairs. Medical Information and the Validation of Promotional Materials. Medical and Technical Writing. Readability testing of Pack Insert Leaflets. For the Pharmaceutical Industry. European Drug Regulatory Affairs. Readability testing of Pack Insert Leaflets. Medical and Technical Writing. Supervision of Medicines Promotion. Medical Information and Publicity. Has access to an effective pa...

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Archemin | Advice & reporting for the chemical and pharmaceutical industries | mpi-bvba.com Reviews

https://mpi-bvba.com

Skip to main content. Advice and reporting for the chemical and pharmaceutical industries. European Drug Regulatory Affairs. Medical Information and the Validation of Promotional Materials. Medical and Technical Writing. Readability testing of Pack Insert Leaflets. For the Pharmaceutical Industry. European Drug Regulatory Affairs. Readability testing of Pack Insert Leaflets. Medical and Technical Writing. Supervision of Medicines Promotion. Medical Information and Publicity. Has access to an effective pa...

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e-CTD and NeeS generation | Archemin

http://mpi-bvba.com/services/e-ctd-and-nees-generation

Skip to main content. Advice and reporting for the chemical and pharmaceutical industries. European Drug Regulatory Affairs. Medical Information and the Validation of Promotional Materials. Medical and Technical Writing. Readability testing of Pack Insert Leaflets. E-CTD and NeeS generation. The electronic Common Technical Document (eCTD) is an interface for the pharmaceutical industry to agency transfer of regulatory information. The eCTD has five modules. 2 Common Technical Document Summaries. BVBA ARC...

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Careers | Archemin

http://mpi-bvba.com/careers

Skip to main content. Advice and reporting for the chemical and pharmaceutical industries. European Drug Regulatory Affairs. Medical Information and the Validation of Promotional Materials. Medical and Technical Writing. Readability testing of Pack Insert Leaflets. Administratief Assistent - Medisch Secretariaat (m/v) (Expires on 31/08/2016. Deadline for application expired. Clinical Research Associate Safety Officer. Medical Writer for the Market Access Unit. At] archemin [dot] eu. You will be required ...

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Medical Information and the Validation of Promotional Materials | Archemin

http://mpi-bvba.com/services/medical-information-and-validation-promotional-materials

Skip to main content. Advice and reporting for the chemical and pharmaceutical industries. European Drug Regulatory Affairs. Medical Information and the Validation of Promotional Materials. Medical and Technical Writing. Readability testing of Pack Insert Leaflets. Medical Information and the Validation of Promotional Materials. Art 98 of Directive 2001/83 as amended require Holders of Marketing Authorisation for Medicinal Products to appoint a Responsible Person for Medical Information. Documentation of...

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Our services | Archemin

http://mpi-bvba.com/services

Skip to main content. Advice and reporting for the chemical and pharmaceutical industries. European Drug Regulatory Affairs. Medical Information and the Validation of Promotional Materials. Medical and Technical Writing. Readability testing of Pack Insert Leaflets. European Drug Regulatory Affairs. Readability testing of Pack Insert Leaflets. Medical and Technical Writing. Supervision of Medicines Promotion. Medical Information and Publicity. BVBA ARCHEMIN - Lange Nieuwstraat 1, 2800 Mechelen, Belgium.

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European Drug Regulatory Affairs | Archemin

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Skip to main content. Advice and reporting for the chemical and pharmaceutical industries. European Drug Regulatory Affairs. Medical Information and the Validation of Promotional Materials. Medical and Technical Writing. Readability testing of Pack Insert Leaflets. European Drug Regulatory Affairs. First-rate Regulatory Affairs services for the Pharmaceutical Industry. National, Mutual Recognition and Decentralised Procedures. Type I and II Variations, 5-year Renewals, Line Extensions.

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BioReg Consultancy - Management Consultancy for biopharmaceutical companies: Network

http://www.bioreg-advice.de/network.html

BioReg Consultancy’s international network of experts comprises:. With the main focus on development, regulatory affairs and GMP inspections for biopharmaceuticals. Pauels Consulting, Germany. With the main focus on nonclinical development of biopharmaceuticals. Pharmitas Ltd, Jon Betts, United Kingdom. With the main focus on UK manufacturing and QP batch release. Archemin bvba, Belgium. With the main focus on regulatory affairs in the Benelux region. Judy Atkins, USA.

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BioReg Consultancy - Management Consultancy for biopharmaceutical companies: Network

http://www.bioreg-advice.com/network.html

BioReg Consultancy’s international network of experts comprises:. With the main focus on development, regulatory affairs and GMP inspections for biopharmaceuticals. Pauels Consulting, Germany. With the main focus on nonclinical development of biopharmaceuticals. Pharmitas Ltd, Jon Betts, United Kingdom. With the main focus on UK manufacturing and QP batch release. Archemin bvba, Belgium. With the main focus on regulatory affairs in the Benelux region. Judy Atkins, USA.

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Skip to main content. Advice and reporting for the chemical and pharmaceutical industries. European Drug Regulatory Affairs. Medical Information and the Validation of Promotional Materials. Medical and Technical Writing. Readability testing of Pack Insert Leaflets. For the Pharmaceutical Industry. European Drug Regulatory Affairs. Readability testing of Pack Insert Leaflets. Medical and Technical Writing. Supervision of Medicines Promotion. Medical Information and Publicity. Has access to an effective pa...

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