I will write gmp sops, quality documents and procedures

Need clear and well structured GMP or quality documentation for your pharmaceutical or medical device operations?

I provide professional support with GMP, quality and technical documentation based on applicable requirements and industry guidance.

I can assist with:

Standard Operating Procedures (SOPs)

Quality Assurance and Quality Control

GMP documentation

Manufacturing processes

Deviations and nonconformances

CAPA

Change control

OOS documentation

Raw material handling

Recall procedures

Validation documentation

Site Master File support

Document and record control

Medical device quality documentation

My background includes pharmaceutical sciences, Regulatory Affairs, Quality, CMC, GMP and medical devices, giving me an understanding of both the scientific and regulatory aspects of technical documentation.

Each project is tailored to your product, market and specific requirements.

Please contact me before ordering so we can discuss your documentation needs.