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What We Write

Validation Protocols

Receive best of practice, highly comprehensive validation protocols for systems such as equipment and utilities, among others.

Standard Operating Procedures

Draw on our wealth of experience to develop SOPs that ensure your processes produce products that comply with your company standards.

Requirement Specifications

Take advantage of our insights and hard-earned knowledge to establish sound rationale behind your tests and acceptance criteria.

 
 
 

Risk Assessments

Work shoulder-to-shoulder with us as we help you identify potential hazards and obstacles, and institute proven new risk controls. Performing risk assessments will also help you determine what tests must be performed during your qualification procedure.

Quality System Policies

Communicate your quality system policy in a way that motivates and ensures both your employees and customers. Our experienced writers can show you how…or do it for you.

 

7 Steps to Write Your Draft


Quality at a Very Competitive Price.

From writing your cGMP documents to consulting on your validation activities, Protocol Writers will give you best service at competitive prices.

Contact us now so we can discuss a quote that will fit your needs.

+1 (415) 854 0320

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We are Protocol Writers and We Write Quality.

We assist pharmaceutical companies to write reliable,
fast and superior validation protocols and quality documents.