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Comprehensive documentation to ensure compliance, efficiency, and clarity in pharmaceutical and biotech operations.
Our technical writing services provide pharmaceutical and biotech companies with clear, precise, and compliant documentation.
From regulatory filings and standard operating procedures (SOPs) to validation reports and technical manuals, we ensure that your documentation meets the highest industry standards.
Our experienced team works closely with your organization to create well-structured, comprehensive documents that help maintain compliance with regulatory bodies like the FDA, EMEA, and GMP, and streamline internal operations.
At CPH Pharma, we understand that each company has unique documentation needs.
Whether it’s creating user manuals for equipment, developing validation documentation, or drafting compliance reports, we tailor our technical writing services to meet your specific requirements.
Our team is experienced in a wide range of documents, ensuring that your materials are not only compliant with regulatory standards but also clear, consistent, and easy to understand for internal teams and regulatory authorities alike.
We provide comprehensive support throughout the documentation process, ensuring that all documents are accurate, well-organized, and comply with all relevant regulations.
From writing and editing to formatting and final approval, our team ensures that your technical documents are ready for submission and audit.
By focusing on detail, accuracy, and compliance, we help you avoid costly mistakes, improve operational efficiency, and maintain a high standard of documentation across all aspects of your business.
Let our team of expert technical writers help you create clear, accurate, and compliant documentation for your pharmaceutical and biotech operations. We’ll work with you to ensure that your technical materials are efficient, regulatory-compliant, and ready for submission or audit.
Contact us today to discuss your technical writing needs and receive customized solutions for your business.
Pharma & biotech compliance experts
GMP, FDA, and EMEA certified
Custom strategies for every project
14+ years of industry success
With over 14 years of experience in the pharmaceutical and biotech industries, we have developed a deep understanding of regulatory requirements and the importance of precise, well-written documentation.
Our technical writers are experts in GMP, FDA, and EMEA standards, ensuring that your documents meet compliance and industry best practices.
Whether you need technical manuals, validation documents, or compliance reports, we provide solutions that enhance your operations and reduce risk, ensuring that your business is always ready for audits and inspections.
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