Operations at Hiranis Pharmacueticals are based on the most modern and meticulous techniques and our manufacturing facility is constructed on the pretext of controlling cross contaminations, ensuring smooth flow of personnel and materials, provisioning optimum environment and assuring worker welfare and safety.
Our state of the art manufacturing facility is a depiction of our progressive vision. Having a state of the art HVAC system, we guarantee the best possible environment for our workers and ultimately our products.
The HVAC system was designed according to cGMP regulations and production requirements. The system was validated by an independent engineering company and Ministry of Health-Pakistan.
Hiranis Pharmacueticals produces specialty products at its state-of-the-art formulation plant. These include solid and liquid oral dosage forms (tablets, capsules, syrups and suspensions).
A highly qualified and trained team of scientists, pharmacists, chemists and engineers work in our Research & Development and Operations departments, developing new products in an environment that celebrates continuous improvement in quality.
Technical staff at Hiranis Pharmacueticals is well versed with contemporary manufacturing techniques and boasts impressive experience of technical operations.
Hiranis Pharmaceuticals has a state-of-the-art production facility designed to facilitate the production of the highest quality products. Hiranis Pharmaceuticals adheres strictly to the principles of cGMP with its modernized production facilities, efficient production control, quality assurance, industrial safety, occupational health and environmental control systems.
Hiranis Pharmaceuticals has always strived in technological advancement, upgrading and expanding its manufacturing plants, heating, ventilation and air conditioning systems (HVAC), production, quality control equipment's & systems in order to attain the cutting edge of excellence and to remain competitive in quality and productivity.
We take precautions to ensure that all facilities, from design to maintenance, follow the highest international standards. Cross contamination at any level is avoided by quarantined production blocks with independent air systems.
We have following Manufacturing facilities at our factory.
Tablet manufacturing
Capsule manufacturing
Liquids manufacturing
Granules for suspension manufacturing
Hiranis Pharmacueticals quality control and quality assurance departments work simultaneously to ensure consistent quality of the product throughout its shelf life.
Hiranis Pharmacueticals is committed to complete customer satisfaction through cost effective products and services of world class quality & delivery to its customer requirements.It is not just what we do , but the way we do it. The Measurement of Quality is how well meet an customer requirements. We seek to ensure that our products consistently meet the highest industry standards and requirements.
Hiranis QC laboratory is equipped with the latest & efficient machinery. Among the list of highly advance and sophisticated QC instrument, some of them are as follows :
| Atomic Absorption Spectrometer | HPLC | Magnetic Stirrer |
| UV Spectrophoto Meter | F.T.I.R | Dissolution Apparatus |
| Disintegration Apparatus | Hardness Tester | Friability Apparatus |
| Oven | Karl Fisher | pH Meter |
| Conductivity Meter | Analytical Balance | Moisture Balance |
| Visco Meter | Polari Meter | Refrectro Meter |
| Melting Point App | Autoclave | Microscope |
| Filtration Assembly | Cool Incubator | Water Bath |
| Oven | Incubator | Vacuum Oven |
| Laminar Flow Cabinet | Fuming Hood | Refrigerator |
| Muffle Furnace | Particle Counter | Colony Counter |
| Eye Shower | Centrifuge Machine | Ultra Sonic Bath |
| Stability Chamber (Climatic Chamber) |
Everyone in the team involved in developing the product is responsible for quality assurance. Hiranis Pharma takes pride in being recognised as a quality conscious organisation. Quality products have been our major strength in achieving success and recognition. Hiranis Pharma has a specialized Quality Assurance department that is dedicated, as the name implies, to assure quality products. But quality assurance does not mean to carry out few analytical procedures in laboratory during the production cycle, but it is a continuous process.
At Hiranis, Quality Assurance means totality of arrangement for quality drugs which includes cGMP Compliance Monitoring at Production, Quality Control, Utilities, Material Management, Administration & Regulatory Compliance which has direct & indirect impact on product Quality, Safety, Purity & Efficacy.
QA has emphasis upon Analysis of Data through Annual Product Review (APR), Quality Risk Management (QRM), Handling & Investigation of Compliant, Deviation & Change Control, Self Inspection/Technical Audit & cGMP Training Plan to Worker & Executive Staff. QA has microscopic role at Hiranis & everything has to pass through it.
Regulatory Affairs (RA) is one of profession in pharmaceutical industry with great potential and opportunities. We have two sub divisions of our Regulatory Affairs Department i.e. DOMESTIC and INTERNATIONAL. In Hiranis Pharmaceutical regulatory department performs the following operations :
Collecting data , analyzing, preparing and presenting documents for registration to DRAP in Pakistan and Regulatory agencies of exporting countries and perform all subsequent dialogue to gain and maintain marketing authorization (MA) for the Pharmaceutical products or health care product.
To Ensure that company comply with all of the regulations and laws according to GMP/cGMP and Drug Law.
To Handle the matters with CDL and DTL laboratories in order to response of their queries/requirements.
To suggest the company regarding regulatory affairs climate that would affect proposed activities. describing the "regulatory climate" around issues like the promotion of prescription drugs compliance.
Preparation of dossiers for exporting countries as per CTD/ACTD format or respective guidelines.
GMP/Free Sale Certification and enforcement actions.
Maintenance and Update of Product Master Files.
Internal Compliance of Documentation.
Coordination with all technical operation departments and marketing department.
Intellectual Property Rights(Trademark).
Business Development activities.
Packaging development (artwork).
