I will prepare ctd modules and cmc regulatory documents

Maissa

Algeria

I speak English, Arabic, French

9 orders completed

Meet Assia, a highly skilled pharmacist with a passion for writing, research, and the pharmaceutical world. With experience in both healthcare, pharmaceutical, compounding, cosmetic formulation, and w...
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About this Gig

Are you looking for reliable support in preparing regulatory documents for pharmaceutical products or medical devices?

Im a pharmacist with regulatory affairs experience, offering professional assistance in preparing, reviewing, and formatting regulatory documents aligned with international guidelines.


I can support you with:

  • CTD / eCTD document preparation and formatting
  • IND and NDA documentation support
  • SOPs, policies, and quality documents (GMP)
  • Pharmacovigilance documents (PSURs and safety reports)
  • Regulatory document review and compliance checks
  • Labeling and packaging compliance review
  • Bilingual support (English and French)



 Ideal for

  • Pharmaceutical companies
  • Medical device companies
  • Startups and regulatory professionals
  • Startups and small to medium-sized companies 


Please contact me before placing an order to discuss your requirements.

For larger projects (full CTD modules, specifically module 03 or submissions), custom offers are available.

Note: I provide support in document preparation and review only. I do not submit documents to regulatory authorities.



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prepare ctd modules and cmc regulatory documents
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Document type:

Documentation

•

Reports

Industry:

Medical & biotech

Language:

English

•

French

Delivery style preference

Please inform the freelancer of any preferences or concerns regarding the use of AI tools in the completion and/or delivery of your order.

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