The pharmaceutical and medical device industries are some of the most heavily regulated sectors globally and for a good reasonProducts manufactured in these industries impact people’s health and well-being directly. The big Regulatory organizations including but not limited to the FDA (Food and Drug Administration) in the U.S., the EMA (European Medicines Agency), and the ISO (International Organization for Standardization), TGA (Therapeutic Goods Administration), MHRA (Medicines and Healthcare products Regulatory Agency), CDSCO (Central Drug Standard Control Organisation), ANVISA (Agência Nacional de VigilânciaSanitária), WHO all require companies to demonstrate that their facilities meet rigorous operational standards.
If your product is contaminated or does not meet safety standards, you may need to recall it, leading to financial losses and reputational damage.
Non-compliance can result in fines and potential shutdowns.
Faulty equipment or contamination can cause unsafe products to reach the market, endangering patients’ lives.
If the product does not meet the necessary standards, it could result in legal action thereby restricting market access in the future.
Persistent non-compliance with CQV standards can lead to the revocation of operational licenses, halting production and impacting business continuity.
Failure to meet CQV standards often results in closer scrutiny more frequent regulatory checks, audits, and rigorous oversight of future operations.
Insufficient CQV can cause disruptions like unplanned downtime, production delays, and higher operational costs.
CQV helps prevent these issues by ensuring that your equipment and processes are in perfect working order, from day one of operation.
Commissioning, Qualification & Validation (CQV) is an integral part of the life sciences and pharmaceutical sector. It is a very detail-oriented process that requires the right mix of knowledge, experience and diligence to correctly place Facilities/Equipment/Utilities into use.
The main difference between Commissioning and Q&V are the guidelines followed. Commissioning is an exercise made from a Good Engineering Practice (GEP) point of view. Q&V is an exercise made from a Good Manufacturing Practice (GMP) point of view.
The objective of CQV process is to demonstrate that a system was designed, installed and performs as per design requirements and/or for its intended use:
Non-critical Facilities/Equipment/Utilities will only require commissioning before being used, as they do not impact on quality.
The International Society for Pharmaceutical Engineering (ISPE) has provided over the years several guidelines on how Qualification &Validation activitiesshould be implemented. Within their guidelines, one of the most widely used Lifecycle Development models is the “V” Model, which is a framework or structure for undertaking the design, execution, commissioning and qualification of a design project. It was first promoted by the International Society of Pharmaceutical Engineers (ISPE) back in 1994 in the first edition of their Good Automated Manufacturing Practices guideline (GAMP).
The “V” Model creates a solid basis for testing the functionality of the system against the original design specifications and proving that the delivered technical solution achieves the desired outcome.
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