Is your company prepared to ANVISA audits and requirements?
- Pre-assessment of the quality system
- Regulatory risk mapping
- GMP/GMP compliance roadmap
- Support from a senior specialist
Risks that cost your operation dearly.
Small failures in the quality system can lead to fines, recalls and suspension of activities.
Recurrent non-conformities
Failures in internal and external audits
Suppliers not adequately qualified
Regulatory and operational risk
Lack of structure in the quality system
Experts who understand the reality of the pharmaceutical industry.
More than a decade structuring quality systems, conducting audits and preparing companies for regulatory inspections.
Strategic vision
Analysis focused on results and risk mitigation — not on a checklist.
Practical action
Team with real experience on factory floors and pharmaceutical laboratories.
GMP/GMP Compliance
Mastery of ANVISA requirements and international quality standards.
Two ways to shield your operation.
Choose the type of audit your company needs now.
Quality Audits
- Assessment of processes and procedures
- Deviation analysis and CAPAs
- GMP compliance check
- Preparation for ANVISA inspections
Supplier Audits
- Supplier qualification
- On-site or documentary assessment
- Reducing risks in the production chain
- Compliance with regulatory requirements
More than compliance.
Regulatory intelligence.
We do not deliver generic reports. We deliver strategic clarity about the real risks of your operation — and the path to mitigate them.
Avoid regulatory risks and be prepared for audits.
Speak to a TB Pharma specialist and receive an initial diagnosis of your operation.
Consultancy specializing in quality and supplier audits for the pharmaceutical industry.
Services
Contact Us
- (11) 99999-9999
- contato@tbpharma.com.br
