I will provide pharma QA documents for usfda , eu approved pharma plant

I am a Pharma QA Documentation Specialist with strong experience in handling regulatory audits and compliance requirements. I have successfully worked on Schedule M documentation and have faced EU and US FDA audits, ensuring complete audit readiness.

My Services Include:

• SOP writing, review, and updates
• Batch Manufacturing Record (BMR) review
• QA documentation and compliance checks
• Schedule M documentation revision
• Audit preparation support (EU & US FDA)
• QA schedule and document management

Why Choose Me?

• Experience in real regulatory audits (EU & US FDA)
• Strong knowledge of GMP and compliance standards
• Focus on accuracy, clarity, and audit readiness
• Reliable and professional communication

Who Can Benefit?

• Pharma companies
• Startups and small manufacturers
• QA teams needing documentation support
• Companies preparing for audits