
Pharmaceutical Industry
- Industries
- Pharmaceutical Industry
Pharmaceutical Industry
The pharmaceutical industry is responsible for all activities related to research, production, and sale of pharmacologically active raw materials (both synthetic and extractive), pharmaceutical formulations for human and veterinary use, diagnostic products, and vaccines. Propharmabi provides comprehensive and integrated support to this sector, offering solutions for all phases of pharmaceutical production with a strong focus on compliance with current regulations and the highest standards of safety, reliability, quality, and efficiency.
In the pharmaceutical industry, the manufacturer’s reputation and, most importantly, patient well-being largely depend on the purity of the products released to the market. For this reason, one of the biggest challenges in this sector is identifying and controlling potential sources of contamination at every stage of the entire production process. Contamination can originate from the working environment, raw materials, processing equipment, and production personnel. Therefore, every operational procedure must take place in controlled contamination environments, such as cleanrooms. From raw material processing to filling, sealing, labeling, and inspection, each production stage must meet strict environmental control standards.

Areas of Intervention
Production Departments
- Oral solid forms (tablets, capsules, solutions, and suspensions)
- Oral liquid forms
- Sterile solutions, injectable products in ampoules, cartridges, vials, and pre-filled syringes
- Lyophilized product departments
- Transdermal administration (patches, pre-medicated sterile gauzes, etc.)
- Primary and secondary pharmaceutical packaging departments
- Pharmaceutical warehouses and cold chain management
- R&D Laboratories
- High-potency active pharmaceutical ingredients (HPAPI) departments
Reference Standards
A key aspect of pharmaceutical production is ensuring compliance with Good Manufacturing Practices (GMP). GMP regulations consist of a set of rules, standards, and guidelines that define proper procedures for manufacturing medicines, medical devices, food products, and dietary supplements.
- Good Manufacturing Practices (GMP)
- ICH Guidelines (International Conference on Harmonisation)
- European Pharmacopoeia (Ph. Eur.)
- ISO Standards: ISO 14644, ISO 13485, ISO 14698
Leveraging its extensive technical expertise, Propharmabi designs, develops, and supplies tools and services for controlled contamination environments. These are essential to ensuring the quality of pharmaceutical products in line with the complete concept of good pharmaceutical manufacturing practices and GMP implementation.
Our work in the pharmaceutical industry













