Quality Control - Good Laboratory Practices (GLP)
Excellence in Good Laboratory Practices for reliable and auditable results.
Excellence, Compliance and Reliability in Laboratory Environments
Good Laboratory Practices (GLP) are a set of guidelines that ensure the quality, integrity and traceability of studies carried out in laboratory environments. Based on OECD guidelines and ANVISA requirements, GLPs guarantee that the results generated are reliable, auditable and valid for regulatory purposes.
T&B Pharma offers complete consultancy and training for diagnosis, implementation and maintenance of GLP in physical-chemical and microbiological laboratories, strengthening the quality culture and readiness for national and international audits.
Our GLP Services
Technical diagnosis the laboratory's level of compliance.
Structured deployment of GLP guidelines.
Resource allocation for your project
In-person and online training for technical and management teams.
Development of SOPs, methods and records in accordance with regulatory requirements.
Simulated internal audits for preparation of official inspections.
Validations and Development of Analytical Methods for physical-chemical and microbiological tests
Statistic for validation of analytical methods
Benefits of GLP Implementation
Greater reliability of laboratory data
Reduced errors and rework (OOS)
Strengthening the quality culture
Strengthening Data Integrity
Compliance with national and international regulatory requirements
Preparing for audits and inspections safely
Our GLP Services
Technical diagnosis the laboratory's level of compliance.
Structured deployment of GLP guidelines.
Resource allocation for your project
In-person and online training for technical and management teams.
Development of SOPs, methods and records in accordance with regulatory requirements.
Simulated internal audits for preparation of official inspections.
Validations and Development of Analytical Methods for physical-chemical and microbiological tests
Statistic for validation of analytical methods
Benefits of GLP Implementation
Greater reliability of laboratory data
Reduced errors and rework (OOS)
Strengthening the quality cultureStrengthening Data Integrity
Compliance with national and international regulatory requirements
Preparing for audits and inspections safely
Why is T&B Pharma the right choice for your Quality Control?
GLP specialists focused on quality, traceability and performance. We operate in an integrated manner. From diagnosis to training, applying ALCOA+ principles for reliable and sustainable results.
Laboratory Challenges, T&B Pharma Solutions
- Difficulty maintaining regulatory compliance?
We implement a complete and efficient GLP system, ensuring adherence to the requirements of ANVISA, OECD and international GxP standards.
- Inconsistent results and constant rework?
We restructure flows and procedures to eliminate failures, reduce OOS and strengthen end-to-end traceability.
- Lack of integration between methods, records and team?
We design unified processes that connect data, documents and responsibilities, promoting efficiency and collaboration.
- Close audits and little internal preparation?
We prepare your team with simulated audits, document reviews and CAPA plans that increase confidence in inspections.
- Need for stronger quality culture?
Through practical training and technical support, we help to consolidate a solid culture of good laboratory practices.
Who Should Adopt GLP?
Laboratories that carry out studies with regulatory impact, such as:
- Pharmaceutical, cosmetic, excipient, API and medical device quality control
- Development of cosmetic and chemical products
- Research and innovation laboratories
