OUR FACILITIES
1. Registration 
•	Arranging drug registration application dossiers in required CTD format and in standards of Ministry of Health. 
•	Converting drug registration dossiers (including those which were previously licensed) from NTA to CTD format.
•	Arranging borderline product registration application dossiers in accurate borderline product dossier format. 
•	Competing with time for owner of registration application; Presenting professional consultancy facility of whole registration (starting  from preparation of registration dossiers to licensing stage).
2. Pharmacovigilance 
3. Organization of Bioavailability –Bioequivalence studies  
4. Pharmaco- Economy: (Pricing and Refunding)
5. Audit
6. Consultancy 
•	Consultancy facilities on regulations, registration, quality, GMP, GLP, GCP practices, pharmacovigilance and other technical subjects on which knowledge is required.

Vg-Far CRO Ltd. Co.

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