Manufacturing and Tech Transfer​

​​​We know how critical cGMP documentation and requirements are and that is where our team of skilled Technical Writing experts can help you during your manufacturing and tech transfer activities. We can provide support in drafting, editing, and reviewing technical documents such as facility fit, process description(s), manufacturing batch records, protocols, summary reports, specifications, SOPS, and manuals. We can provide support for the development of technical documents for Manufacturing, Engineering, Clinical Operations, Global Harmonization, Regulatory Affairs, and more.