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Validation Service

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Why CPPL

CPPL has a highly skilled GMP team supported by engineers. Since CPPL is renowned for its proficiency in the GMP sector, we are knowledgeable about regulations and comprehend what is needed.CPPL Facts regarding the cost-cutting element. CPPL advises clients on when and when not to make concessions. Instead of working on a commission structure, CPPL uses lump sum consultancy fees, which spares clients from needless stress and prevents project extensions.Whether or not it is covered under the contract, we don't care; instead, we recommend reputable vendors to our clients, assist them in selecting the right equipment, and support them in negotiating lower costs for fabrication, AHU systems, and other items. As experts, we have designed over 15 plants in India to date and have helped other manufacturers with technical guidance about changes and technical aspects.

Our Validation Service

Process Validation is a crucial aspect of Pharmaceutical Manufacturing. Manufacturers possess proficient personnel, staff, and technocrats who can handle Process Validation activities. However, we have noticed that many auditors and authorities find loopholes in Process Validation documents that cannot be fixed, leading to audit failure.
In order to save time and prevent future problems with regulatory compliance, CPPL has experts who design process validation protocols in accordance with your specifications and provide guidance on how to carry them out. Additionally, after an activity is completed, our team reviews the entire document and makes suggestions or requests that any errors be corrected.

CPPL designs process validation protocol.
CPPL Gives sampling points and testing plan for execution of process validation.
CPPL team executes also entire process validation activities.
CPPL team compiles report and submit to the manufacturers.
CPPL team reviews report which manufacturer has prepared and suggest the changes according to need.

CPPL helps you in:

Designing Qualification protocols.
Assist in filling Qualification reports.
CPPL Executive are able to visit your site and execute entire qualification activity.
CPPL Provides protocol and reviews report of manufacturers.
CPPL helps in getting all certification from vendors.
CPPL helps in SAT, FAT Activities.

  • Process Validation
  • Analytical Method Validation
  • Process Improvement
  • Validation Training
  • Validation Documentation
  • Product Monitoring

Cyclone Pharmaceuticals Provide CSV Validation in both segments i.e Computer System and Computerised System validation in the light of latest regulatory Guidelines

Benefits Of Service

Provide 100 % assured CSV service

  • System Validation
  • Software Validation
  • PLC Validation
  • ERP validation
  • QMS Validation
  • CSV Documentation
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