Facility
Our products are manufactured at state-of-the-art manufacturing facilities, well-equipped with the latest technological plant and machinery. All the facilities have WHO-GMP certification and the ISO 9001:2015 certifications.
High-quality raw materials are used as per approved WHO guidelines. In-process quality controls are implemented to check and maintain finished product quality. Finished products are randomly checked or analyzed at independent laboratories to assure their quality.
We ensure that our products conform to international standards of quality, efficacy, and safety. Bohra Lifescience strictly and meticulously adheres to guidelines from pharmacopoeias while designing and developing formulations. We consistently deliver enhanced value to our customers through personnel training and continuous improvement of processes, products, and practices.
Details
Our partner manufacturing facility has end-to-end capabilities:
- Lab scale development to pilot scale up
- Commercializing the product for large-scale manufacturing and global marketing
We manufacture dosage forms of:
- Tablets: Uncoated Tablets, Film Coated Tablets, Multi-Layer Tablets, Enteric Coated Tablets, Sugar Coated Tablets, and Dispersible Tablets.
- Liquid Orals: Multivitamin Syrups, Cough Syrups, Antacids.
Location
The manufacturing facility is located in Roorkee, Uttarakhand, near Haridwar, a religious city approximately 200 kilometers away from India’s capital, New Delhi. Good climatic conditions, easy availability of raw and packing materials for regular production, and excellent infrastructure facilities make its location ideal for pharmaceutical manufacturing in India.
Certification
The manufacturing unit has been accredited with WHO-GMP Certification. Personnel in the facility strictly follow the WHO-GMP guidelines in the production areas to achieve the best quality in pharmaceutical products.
Quality Control
Our manufacturing facility is well-equipped with the latest industry standards. The Quality Control department has the latest testing equipment and well-qualified staff. The lab holds GLP (Good Laboratory Practices) certification from our FDA.
Our R&D Capabilities
Our experienced team of Research & Development personnel specializes in:
- Formulation development
- Process development and validation
- Analytical development
- In-process quality control
- Quality Assurance, conducting stability studies, and dossier development
Eco-friendly policies: The plant has a proper waste management system, with water disposal done through an ETP system. We maintain more than 30% green area in our factory premises.
Capacity
Our plant has an installed capacity of 180 million tablets and 2 million bottles of syrup/suspension per month on a one-shift basis, and this capacity can be further increased as per requirement.
Packaging
The plant is equipped with customized packaging machines to cater to customer needs and employs cutting-edge technology with innovative solutions.