Good Laboratory Practice (GLP)
At ComplyPlanet, we help organizations in pharmaceuticals, biotechnology, chemicals, agro-sciences, medical devices, and related sectors achieve and sustain Good Laboratory Practice (GLP) compliance. We understand that data integrity, traceability, and scientific rigor are at the heart of reliable non-clinical studies. GLP is the framework that ensures your laboratory results stand up to regulatory scrutiny.
Our GLP consulting services are designed to help you implement quality systems that ensure the accuracy, reproducibility, and integrity of data generated from your laboratory studies.
Whether you are setting up a new lab, scaling operations, or preparing for inspections, we provide practical guidance to embed GLP principles into your day-to-day processes and culture.
By working with ComplyPlanet, you can:
- Design and implement GLP-compliant quality management systems and documentation
- Develop robust Standard Operating Procedures (SOPs) for study planning, execution, reporting, and archiving
- Ensure data traceability, security, and integrity across all laboratory activities
- Establish clear roles, responsibilities, and accountability for lab personnel
- Build a culture of good documentation, accuracy, and ethical study conduct
- Reduce the risk of regulatory findings, data rejection, or study invalidation
Whether you are targeting national or international GLP standards (such as OECD GLP, US FDA GLP, or Indian GLP Certification), ComplyPlanet provides comprehensive, business-friendly solutions to help you achieve and maintain compliance.
Why Choose ComplyPlanet for GLP?
- End-to-end support: From gap assessments and SOP development to internal audits and inspection readiness
- Tailored solutions: Customized to your laboratory type, study scope, and regulatory requirements
- Regulatory insight: We help you stay aligned with evolving GLP guidelines and expectations
Connect with Our GLP Compliance Experts!