1) 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.

2) 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.

3) To provide training for pharmaceutical or guideline updates to enhance their understanding.

4) Assistance is offered in drafting responses to Drug Master File (DMF) or Agecy or client queries, incorporating scientific rationale.