Our Facilities
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Manufacturing Facility
The first state-of-the-art soft gelatin capsule manufacturing facility in the UAE.
Installed Capacity
1.5B Capsules
Per Annum
Packed in blister and bottle format
Tha largest facility in the region with
23K sq.m Plot Size
Centrally Located in Dubai, UAE
Maria O’Neil
At Bioventure Healthcare, our mission is to improve the health and well-being of patients worldwide. We are committed to achieving this mission by developing innovative and effective drugs that meet the unmet medical needs of patients. As part of our commitment to quality and innovation, we have been expanding our operations in recent years, and we are excited to announce that we are currently constructing a fully integrated Oral Solid Dosage (OSD) section on-site.
We believe that this new facility will help us to achieve our goals of increasing production capacity, improving efficiency, reducing costs, and enhancing the quality of our products.
Bioventure Healthcare is committed to improving the health and well-being of patients worldwide.
The new fully integrated Oral Solid Dosage (OSD) section is a significant investment that highlights the company’s commitment to excellence.
The company is committed to providing the highest level of care to its patients and will continue to grow and expand to meet the needs of patients worldwide.
Currently Constructing a Fully Integrated Oral Solid Dosage (OSD) Section on-site
Bioventure Healthcare is a pharmaceutical company that is focused on developing innovative and effective drugs to meet the unmet medical needs of patients worldwide. The company has been expanding its operations in recent years, and it is currently constructing a fully integrated Oral Solid Dosage (OSD) section on-site. This new facility is set to be a major milestone for the company and will help to improve its manufacturing capabilities significantly.
Product Library
Step 1
Production Facility
- Compliant to current cGMP requirements and meeting all international standards
- High-speed encapsulation ensuring high quality soft gelatin capsules
- Symetix Automatic Inspection system
Step 2a
Blister Primary Packing
- Compatible with all packing materials and complies with 21CFR Part 11
- Equipped with a No-Fill Detection (NFD) system to automatically detect faulty strips
Step 2b
Blister Primary Packing
- Dedicated lines for bottle filling with capping, induction sealing and bulk capsule packing options
Step 3
Secondary Packing
- High-capacity auto- cartonator compliant with 21 CFR Part 11, with a camera detection system for barcode and over printing details
- Tamper-evident serialization system providing Track and Trace capability for regulatory compliance and better brand protection
Step 4
Stability Chambers & Microbiology Lab
- State-of-the-art microbiology lab
- Walk-in stability chambers simulating climatic zones
Step 5
Quality Control Lab
- Fully compliant with all cGMP requirements
- Compliant with 21 CFR Part 11
- Capable of performing analytical method transfer, method validation, analysis and release of raw material, and analysis of packaging and finished products of various dosage forms
A Glimpse into Our Pharmaceutical and Supplement Manufacturing, Packaging and Quality Control Workflow
1. Production Facility
- Compliant to current cGMP requirements and meeting all international standards
- High-speed encapsulation ensuring high quality soft gelatin capsules
- Symetix Automatic Inspection system
2a. Blister Primary Packing
- Compatible with all packing materials and complies with 21CFR Part 11
- Equipped with a No-Fill Detection (NFD) system to automatically detect faulty strips
2b. Bottle Primary Packing
- Dedicated lines for bottle filling with capping, induction sealing and bulk capsule packing options
3. Secondary Packing
- High-capacity auto- cartonator compliant with 21 CFR Part 11, with a camera detection system for barcode and over printing details
- Tamper-evident serialization system providing Track and Trace capability for regulatory compliance and better brand protection
4. Stability Chambers & Microbiology Lab
- State-of-the-art microbiology lab
- Walk-in stability chambers simulating climatic zones
5. Quality Control Lab
- Fully compliant with all cGMP requirements
- Compliant with 21 CFR Part 11
- Capable of performing analytical method transfer, method validation, analysis and release of raw material, and analysis of packaging and finished products of various dosage forms
GMP Standards
