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On Site Supports
- The execution of analytical method validation on site as per requirements with their GLP scope and provide the documents including the method validation protocols, reports, and annexures.
- Quality personnel are guided to prepare standard operating procedures (SOPs) and standard test procedures (STPs) to ensure complianceTraining-related knowledge updation to Staff for better understanding.
- To provide training for pharmaceutical or guideline updates to enhance their understanding.
- Assistance is offered in drafting responses to Drug Master File (DMF) or Agecy or client queries, incorporating scientific rationale.
