I will prepare gmp sops, sanitation procedures, batch records, and qc forms


About this gig
GMP compliance requires more than having products ready for sale. Your business should have clear procedures for production, sanitation, quality control, batch records, raw materials, complaints, recalls, and document control.
I prepare structured GMP documents for brands and manufacturers that need practical quality records for production readiness, supplier requirements, internal control, and audit preparation.
I can prepare:
- GMP SOPs
- Sanitation Procedures
- Batch Record Templates
- Quality-Control Forms
- Raw Material Record
- Production Checklist
- Cleaning Log
- Equipment Maintenance Log
- Complaint Handling Form
- Recall Procedure
- Document-Control Form
This service is suitable for cosmetic brands, skincare businesses, food producers, supplement brands, private-label sellers, small manufacturers, and production facilities that need organized GMP documents instead of generic templates.
Each file is prepared around your product type, production process, facility workflow, quality checks, and current documentation stage, so your GMP records look clear, usable, and audit-focused.
Get to know Sara
ISO 9001 QMS Manual SOPs Audit Documents
- FromUnited Kingdom
- Member sinceJul 2026
- Avg. response time2 hours
Languages
English, French, German
Other Regulatory Compliance Consulting Services I Offer
FAQ
Can you prepare GMP SOPs?
Yes. I prepare GMP SOPs based on your product type, process, and documentation needs.
What documents can you prepare?
I can prepare SOPs, sanitation procedures, batch records, QC forms, cleaning logs, complaint forms, recall forms, and document-control records.
Are the documents customized?
Yes. The documents are prepared around your product, process, facility workflow, and quality checks.
Can these documents support audit preparation?
Yes. They can support internal readiness, supplier review, production control, and audit preparation.
Do you guarantee GMP certification?
No. Certification depends on implementation, facility conditions, auditor review, and certification body requirements.

