Production
Shrooq Pharma’s plant is continously inspected and approved for the production of pharmaceuticals in accordance with cGMP by local and international regulatory authorities. The company has also acquired ISO-9001 OMS Certification strictly following cGMP standards.
Pharmaceutical Formulations
Shrooq Pharma’s core business activity is pharmaceutical formulations which includes product development, manufacturing & marketing. Our product range exceeds over 400 (Registered with Drug Regulatory Authority of Pakistan); in the form of capsules, tablets, syrups, dry powder suspensions, ointments, creams, lotions, eye drops, nasal spray, dry powder injections, ampules and vials. Meanwhile, an anti-cancer section is under development.
The facility includes manufacturing, quality control, quality assurance, research & development, purified air supply, WFi, clean steam generation, canteen, prayer room and administrative department. The plant is designed to minimize chances of product contamination with a state-of-the-art HVAC system.
Quality Control & Quality Assurance
We believe that quality is the main ingredient so at Shrooq Pharma’s quality assurance department runs with the utmost of efficiency, monitoring each & every step of the production process. Quality control is executed in accordance to cGMP, striving to provide high grade quality products.
Quality Control & Quality Assurance
We believe that quality is the main ingredient so at Shrooq Pharma’s quality assurance department runs with the utmost of efficiency, monitoring each & every step of the production process. Quality control is executed in accordance to cGMP, striving to provide high grade quality products.
Dedicated facility for
- Liquid Syrup Section
- General Tablet Section
- Quinolone Tablets Section
- General Capsule Section
- Steroidal Capsule Section
- General Sachet Section
- Eye drops and Nasal Spray Section
- Ointment/Cream and Lotion Section
- Ampule and Small Volume Infusion Section
- Dedicated facility for cephalosporin capsule, dry powder suspension, dry powder injection
- Dedicated Research and Development Section for capsules, tablets, ointments, creams and syrups.
- Oncology Tablet/Capsule and Vial section (under development)
Dedicated facility for
- Liquid Syrup Section
- General Tablet Section
- Quinolone Tablets Section
- General Capsule Section
- Steroidal Capsule Section
- General Sachet Section
- Eye drops and Nasal Spray Section
- Ointment/Cream and Lotion Section
- Ampule and Small Volume Infusion Section
- Dedicated facility for cephalosporin capsule, dry powder suspension, dry powder injection
- Dedicated Research and Development Section for capsules, tablets, ointments, creams and syrups.
- Oncology Tablet/Capsule and Vial section (under development)
Microbiological Lab
- Microbial Testing of sterile drug products
- Microbial Testing of Non-sterile drug products & Raw materials
- Confirmation of contamination free products
- Area monitoring
- Water testing
- LAL test for pyrogen testing
- Media/Broth Fill protocols implementation
R&D Department
- State of the art R&D lab
- Pre-formulation studies
- Excipient compatibility studies
- Analytical method development and validation
- Formulation development
- Stability studies
- Manufacturing process development
- Improving product quality of running products
Microbiological Lab
- Microbial Testing of sterile drug products
- Microbial Testing of Non-sterile drug products & Raw materials
- Confirmation of contamination free products
- Area monitoring
- Water testing
- LAL test for pyrogen testing
- Media/Broth Fill protocols implementation
R&D Department
- State of the art R&D lab
- Pre-formulation studies
- Excipient compatibility studies
- Analytical method development and validation
- Formulation development
- Stability studies
- Manufacturing process development
- Improving product quality of running products