Validation
Validation for Pharma Industry
Sathram Corp has potential experience in handling the validation services for Pharma and Biotech Industry for many years. With an extensive ability to understand the requirements and the compliances of Pharma Industry, we certainly gain the extra edge in providing top notch services to our clients.
Validation is a critical process that ensures that systems, equipment, and processes are designed and operated in a way that meets the required quality standards. Validation plays a crucial role in pharmaceutical manufacturing to ensure the safety, efficacy, and quality of drugs produced.
There are several types of validation processes involved in pharmaceutical manufacturing, including:
- Process Validation
- Equipment Qualification
- Analytical Method Validation
- Cleaning Validation
- Computer System Validation
FAQ's
What is Validation?
Validation is a critical process that ensures that systems, equipment, and processes are designed and operated in a way that meets the required quality standards.
Why is Validation necessary?
It ensures product safety, regulatory compliance, and maintains integrity of IT equipment.
How is Validation performed?
By developing and testing cleaning procedures, and verifying through sampling and analytical methods.
What are the phases of Validation?
Planning, protocol development, testing, and documentation of results.
Who conducts Validation?
The CRO coordinates with quality control and maintenance teams.
