Process Validation
Validation translates to enhanced competitiveness and profitability.
The importance of validating pharmaceutical processes
Validation of pharmaceutical processes is essential to ensure the quality, safety and effectiveness of medicines. This requirement ensures that production processes meet the predefined criteria and comply with good manufacturing practices (GMP).
Ensure compliance and safety
Through strict methodologies, T&B Pharmaminimizing risks e protecting patients' health.
Optimize your pharmaceutical processes
A T&B PharmaReduces waste e Improves Performance of its processes, resulting in resource savings and increased productivity.
Customized solutions
With extensive experience in the pharmaceutical sector, T&B Pharma
From risk analysis to the elaboration of protocols and execution of tests, our specialists work in partnership with your team to ensure the compliance and effectiveness of its processes.
Achieve tranquility and credibility for your company.
By investing in the validation of pharmaceutical processes, you guarantee the tranquility of operating within the standards and Strengthens credibility of your brand before the market.
Demonstrate your commitment to quality and safety, conquering the confidence of customers and partners.
Full Service solutions in validation and qualification for the pharmaceutical industry
Oferecemos um portfólio abrangente de serviços de validação e qualificação para a indústria farmacêutica, garantindo a conformidade com as normas regulatórias, a qualidade dos seus produtos e a eficiência dos seus processos. Nossos serviços incluem:
Validation and qualification in the industry
In the T&B Pharma Consulting, we offer integrated, complete and personalized technical solutions em Validation of production processes, equipment and utility qualification, computed systems validation and statistical analyzes applied to quality. Our goal is to promote sanitary security, regulatory compliance and operational efficiency for industry companies Pharmaceutical, cosmetic, medical devices and active pharmaceuticals (IFA).
We have a team of senior consultants, with national and international experience, to ensure that each stage of the processes strictly meets Good manufacturing practices (GMP), regulations of ANVISA, RDCs, Normative instructions and global demands such as FDA 21 CFR Part 11 and guidelines of I.
Our job goes beyond compliance: we deliver technical intelligence, strategic support and analytical view to raise the maturity level of your production processes, ensuring traceability, reproducibility, risk reduction and increased productivity.
Process Validation
Validation of packaging processes
Qualification of equipment and utilities (DQ, IQ, OQ, PQ)
Computerized Systems Validation (CSV)
Validation of analytical methods-physicochemical and microbiological
Statistics and continuous process verification
Cleaning Validation.
