Medival Technologies

  Standard Operating Procedures for Pharmaceutical In the face of a challenging regulatory environment, we Medival Technologies create a culture where quality objectives are transparent, well understood, and undoubtedly these goals can be achieved by following certain sets of procedures called as “Standard Operating Procedures(SOP)”. Procedures are essential for any plant’s effectiveness and efficiency, and they are regulatory requirement in the Pharmaceutical Industry. A Standard Operating Procedure (SOP) is a set of written instructions that document a routine or repetitive activity which is followed by employees in an organization. A facility manufacturing pharmaceutical products will typically develop, maintain and execute hundreds of SOPs. SOPs are to create the level of quality and accepted practice for a specific procedure. Read more about Products & Services https://medivaltechnologies.com/ ...

  Standard Operating Procedures for Pharmaceutical In the face of a challenging regulatory environment, we Medival Technologies create a culture where quality objectives are transparent, well understood, and undoubtedly these goals can be achieved by following certain sets of procedures called as “Standard Operating Procedures(SOP)”. Procedures are essential for any plant’s effectiveness and efficiency, and they are regulatory requirement in the Pharmaceutical Industry. A Standard Operating Procedure (SOP) is a set of written instructions that document a routine or repetitive activity which is followed by employees in an organization. A facility manufacturing pharmaceutical products will typically develop, maintain and execute hundreds of SOPs. SOPs are to create the level of quality and accepted practice for a specific procedure. Read more about Products & Services https://medivaltechnologies.com/ ...

  ISO 9001:2015 Certified company for validation Being an ISO 9001 : 2015 certified company allows us to expand our market and attract potential customers that may not be familiar with us. ISO Certification guarantees that the organisation is fulfilling the global quality standards. The Certification acts as an assurance that our services are being built in a facility that meets the requirements of ISO. Read more about Products & Services https://medivaltechnologies.com/

  Validation Reports The Validation Report describes in detail the test programme and quantifies all results and measurements. Each page in the report is numbered consecutively and is embossed to prevent duplication. Reports are produced as soon as possible after the work is done and we are always looking for ways in which technology can speed up this process. Read more about Products & Services https://medivaltechnologies.com/

  Validation Protocols Validation Protocol is defined as a documented plan for testing a pharmaceutical product and process to confirm that the production process used to manufacture the product performs as intended. Our protocols include customized validation approaches and methodology with clearly defined, pre- determined acceptance criteria. We offer fast docu-mentation turnaround and can schedule validation projects with short lead times. Principle benefits include reduced cost and time to achieve a compliant system. We use a pragmatic, integrated approach to commissioning and validation activities ensuring sound documented compliance with cGMP for all our assignments. Read more about Products & Services https://medivaltechnologies.com/

  Computerized System Validation (CSV) _______________________________ Computerized Systems (CS) using Programmable Logic Controllers (PLC) are utilized for controlling manufacturing equipment. Such a CS is referred to as a PLC-Based CS (PBCS). Proper workability and operability of CS has become more important to prove that poor quality drugs are not being produced due to the malfunction of CS. The regulatory authorities require drug production companies to prove that their processes and CS that controls such processes, are adequate to produce high-quality drugs, by showing evidence based on documents or electronic data regarding drug development and verification. Medival use a pragmatic, integrated approach to commissioning and validation activities – ensuring sound documented compliance with cGMP for all our assignments. ...