Production Сonsulting
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Implementation of specialized measures aimed at optimizing and developing the production cycle of medicines in accordance with the requirements of GMP of the EAEU
Work Stages

Quality System Audit

Audit plan preparation

Assessment of the quality system, production conditions and quality control of medicines for compliance with the of GMP EAEUrules

Audit results report preparation

CAPA plan and recommendations for improvement development


Technological Support

Solving existing production tasks

Technological processes and analytical techniques transfer

Production and quality system documents creation





Pharmaceutical Substances and Auxiliary Materials Suppliers Audit

Audit plan and questionnaires preparation

Assessment of the quality system, production conditions and quality control of pharmaceutical substances and auxiliary materials manufacturers for compliance with the EAEU GMP rules

Audit results report preparation


Contract Production

Assessment of the contract production placing possibility on the site

Audit of the production site, development of measures to improve the quality system, production conditions and quality control of medicines

Organization and implementation of technology transfer

Production technological support
Contuct Us

Phone/Whatsapp/Telegram
+7 996 716 83 66

E-mail
info@mpmadviser.com

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