FCE Pharma 2026
T&B Pharma naFCE Pharma 2026
Specialists in GMP/GMP/GLP/BPAD, Qualifications and Validations and International Inspections (FDA/WHO/EMA)
Join us during FCE Pharma and discover how your company can adapt to the new regulatory requirements of ANVISA, PIC/S and ICH with more security, traceability and compliance.
T&B Pharma will be present na FCE Pharma
Our technical team will be available at Feira-FCE to talk about your needs and new ANVISA challenges, such as new requirements for compounding pharmacies (production of injectables), equipment qualification requirements for IFA (Annex 15), new revision of RDC 166 (Analytical Methods), and much more, come check it out!
Our focus will be on helping pharmaceutical, cosmetic, veterinary, food and medical device manufacturers reduce regulatory risks and increase operational compliance.
End-to-end technical solutions
Knowledge applied throughout the life cycle of the pharmaceutical product.
Contamination and Sterility Control
Qualification, Validation and QRM
GMP Audits
New Regulatory Requirements
REGULATORY INSIGHTS
Exclusive Technical Insights
Talk to our experts during FCE Pharma and learn about the main trends, regulatory requirements and practical strategies to adapt to the new standards in the pharmaceutical industry.
FEATURED THEME
New Annex 1 PIC/S and CCS Strategy
TECHNICAL DISCUSSION
Media Fill, Sterility and Monitoring
REGULATORY INSIGHTS
RDC 166/2017, ICH Q2(R2) and AQbD
SPECIALIZED CONSULTANCY
Cleanrooms, GMP and Quality Management
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Your data is secure and will only be used for technical/commercial contact with T&B Pharma.
Technical authority on regulatory compliance
GMP and GMP experts
Experience in ANVISA audits
Projects for the pharmaceutical industry
Complete regulatory compliance
Quality management and validation
Multidisciplinary team
Will participate in FCE Pharma 2026
Schedule a conversation with our experts during the fair and discover how to accelerate your company's regulatory compliance.
