We are assisting you to improve your document quality and writing important documents for your manufacturing plant. Documents included but not limited to-
– Letter of Authorization
– SmPC, PIL or Pack insert
– Label and carton contents
– COA, MOA and Specification of Active, Excipients and Finished Products
– Process validation, Stability, PDR & AMV
– BMR / MFR
– Clinical and Toxicity studies
– SOPs for QA, QC & Regulatory departments