I will write ctd ectd regulatory documents and pharmaceutical dossiers
I will do medical writing , regulatory writing and healthcare content
About this Gig
I will write DRAP-compliant CTD/eCTD dossiers for pharmaceutical registrations.
Are you struggling with DRAP observations, incomplete Form-5 or CTD modules?
i help pharma companies in Pakistan and worldwide get their dossier approved fast.
YOU WILL GET :
- Complete CTD dossier (Module 1 to 5 )
- eCTD ready structure
- DRAP Form-5, Form-6, Form-7
- Module 3-Quality, Manufacturing/Stability
- PIL, SPC
- SOPs, BMR, BPR, Specifications.
- variations and renewals
WHY ME?
- 100% DRAP and ICH guidelines compliant.
- Fast turn around, manually written.
- Confidential.
- Worked with tablets, capsules, injectables, infusions, syrups.
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.
FAQ
What do you need to start my dossier?
I need the product name, composition, manufacturing method, stability data, HPLC reports, CoA, and specifications. Message me, and I will send you a simple checklist.
Is it compliant with DRAP?
Yes, 100% as per the latest DRAP CTD guidance and ICH guidelines.

