Script Molecular is a biotech consulting firm based in San Francisco. We are your trusted and knowledgeable partner for solutions in new product development and documentation. We will streamline the process of bringing your product to market. Script Molecular technical writing consultants have been trained by the best in the industry on biomedical regulatory compliance documents for agencies such as the FDA, WHO, MHRA, EMA and IVDR. We are experts in creating, editing, and reviewing technical documents, such as protocols, summary reports, product specifications, SOPs, quality manuals, validation master plans, work instruction, batch records and instructions for use. We also reviews device history files and device master records for medical devices.