WHAT IS GLP - GOOD LABORATORY PRACTICES CERTIFICATION
Good Laboratory Practice or GLP specifically refers to a quality system of management controls for research laboratories and organizations to try to ensure the uniformity, consistency, reliability, reproducibility, quality, and integrity of chemical (including pharmaceuticals) non-clinical safety tests; from physio-chemical properties through acute to chronic toxicity tests. GLP applies to non-clinical studies conducted for the assessment of the safety or efficacy of chemicals (including pharmaceuticals) to man, animals and the environment.
How to get certified in 5 Simple steps
- Fill the Certification Intent Form and send it to us.
We will do a FREE GAP analysis of your organisation with respect to GLP Standard and give you a quote.
- Get Trained and Finish the Documentation work.
Once you have agreed to our quotation, Our team will provide the required trainings to you and will complete the documentation work required for GLP certification.
- Pre-assessment and Internal Audit.
We will then conduct a pre assessment audit to ensure that you organisation meets the desired certification requirements.
- Final Audit by Certification body – Guaranteed Success !
We will provide assistance during final certification audit to ensure that your organisation achieves certification successfully !
- Receive Certificate and Make Payment !
We are a quality conscious organisation and believe in Total Customer Satisfaction. So if you are 100% satisfied and happy with our service, make payment to us.