At Tridev Biosciences, we are committed to delivering high-quality pharmaceutical solutions through state-of-the-art manufacturing and rigorous quality standards.
Located in the heart of Baddi, Himachal Pradesh, we specialize in the production of tablets and capsules, catering to third-party manufacturers and fulfilling government tenders.
With certifications like ISO 9001:2015, GMP, and GLP, we ensure that every product meets stringent industry benchmarks. Backed by a fully equipped Quality Control (QC) laboratory, we uphold excellence at every step of the manufacturing process.
Our state-of-the-art Quality Control Lab is equipped with advanced instruments such as HPLC, UV-Visible Spectrophotometer, Dissolution and Disintegration Apparatus, Friability Apparatus and many more. These tools enable us to conduct precise testing and analysis to ensure every product meets the highest standards of quality, safety, and regulatory compliance.
Our manufacturing process follows a streamlined, quality-driven approach—from sourcing certified raw materials to delivering finished pharmaceutical products. Each step is guided by strict compliance with GMP and GLP standards, ensuring precision, safety, and consistency in every batch.
Sourcing high-grade APIs and excipients from certified vendors, followed by strict QC testing.
Storing raw materials under controlled conditions and accurately weighing/dispensing as per batch requirements.
Uniform mixing or granulating of ingredients to ensure consistency in every formulation.
Manufacturing the required dosage forms—tablets or capsules—using modern equipment.
Continuous monitoring and testing during production to maintain quality and accuracy.
Hygienic packing of finished products with labeling, batch coding, and tamper-proof sealing.
Comprehensive QC analysis of finished goods and QA review before batch release.
Safe storage in a controlled warehouse and on-time delivery to clients with full batch documentation.
We manufacture a wide range of pharmaceutical products including tablets and capsules
Our in-house QC & QA teams conduct rigorous testing at every stage—from raw material procurement to final product release.
MOQ varies based on the product and formulation. Please contact our team to discuss specific requirements and custom batch sizes.
Our processes are designed to comply with WHO, FDA guidelines, supported by robust documentation, validation, and audit readiness.
We have a fully equipped Quality Control lab for physical, chemical, and microbial testing, including HPLC, UV spectrophotometer, dissolution testing, and stability chambers.
Absolutely. We provide contract manufacturing and private label solutions to pharmaceutical companies looking for reliable, high-quality production.
Simply reach out to us via our contact form, email, or phone. Our business development team will guide you through the process and provide a tailored solution.
Yes, we welcome facility visits for our partners and clients. Visits can be scheduled with prior notice and proper safety protocols in place.
