Pharmaceutical Documentation Services

Site Master File We provide services on preparing Site Master File which has brief information about the manufacturing site for pharmaceutical products. The SMF is typically reviewed and updated on regular basis to ensure that it remains current and accurate. It may also be reviewed by regulatory agencies as part…

Standard Operating Procedures We provide Services on preparing Standard Operating Procedures which outlines the steps that needs to be followed to perform a specific task or activity to ensure that tasks are performed consistently and in compliance with regulatory requirements. The portfolio includes, Ware-House Quality Assurance Production Quality Control Microbiology…

Standard Testing Procedures We provide Services on preparing Standard Testing Procedures to evaluate the quality and safety of drugs and other pharmaceutical products. These procedures are designed to ensure that the products meet established standards for purity, strength, stability and other characteristics. The portfolio includes, Quality Control Microbiology Pharmaceutical Documentation…

Quality Manual We provide services on preparing Quality Manuals, which outlines the policies and procedures for ensuring the quality of pharmaceutical products. It is a comprehensive guide that covers all aspects of the manufacturing process, from raw material sourcing and testing to final product release. Pharmaceutical Documentation Services Pharmaceutical Consultancy…

Calibration Master Plan We provide services on preparing Calibration Master Plan, which outlines the process of calibrating the equipment and instruments used in pharmaceutical industry. It includes a list of all equipment that needs to be calibrated, the frequency at which calibration is required and the procedures and standards to…

Validation Master Plan We provide services on preparing Validation Master Plan, which is a high level document which explains about the validation strategy for the compliance requirements. To ensure that the processes, facilities, equipment and systems used to manufacture pharmaceutical products are consistent and meet the required quality standards. We…

Qualification Protocols We provides services in preparing Qualification protocols that outlines the specific procedures and criteria that will be used to qualify equipment, facilities, systems and process in pharmaceutical industry. The portfolio includes Installation Qualification (IQ) Operation Qualification (OP) Performance Qualification (PQ) Pharmaceutical Documentation Services Pharmaceutical Consultancy Services Contact info@pharmaguides.org

Batch Manufacturing/Packing Records We provide services in preparing Master Batch records which has a detailed information of the production and testing of a batch of the pharmaceutical products. They provides a complete record of all the activities performed during the production process, including the materials used, equipments and instruments that…

Training Services On – the – Job (OJT) training, Online webinars will be provided for the individuals in order to develop their knowledge and skills needed to work in this field with minimal risk of errors and improve the quality of their products. Wide range of topics includes: Good Manufacturing…

Medical Writing Services We have extensive knowledge on medical writing services in the following Package Inserts/Information Leaflets Summary of product characteristics (SmPC) Material Safety Data Sheet (MSDS) Content for HealthCare Websites Pharmaceutical Documentation Services Pharmaceutical Consultancy Services Contact info@pharmaguides.org