Our services

Research and Development (R&D): Conducting research to discover and develop new drugs, biologics, vaccines, and other therapeutic products. This includes preclinical studies, clinical trials, and obtaining regulatory approvals.

Manufacturing: Producing pharmaceutical products in various dosage forms such as tablets, capsules, injectables, creams, ointments, and more. Adhering to Good Manufacturing Practices (GMP) and ensuring quality control are essential aspects.
Quality Control and Assurance: Implementing rigorous quality control measures to ensure the safety, efficacy, and quality of pharmaceutical products. This involves testing, validation, compliance with regulatory standards, and continuous improvement processes.

Regulatory Affairs Managing interactions with regulatory agencies worldwide, submitting applications for drug approvals, maintaining compliance with international regulations, and staying updated on global regulatory requirements.

  1. Marketing and Sales: Developing and implementing marketing strategies to promote pharmaceutical products to healthcare professionals, hospitals, pharmacies, and consumers globally. This includes market research, advertising, sales force activities, and distribution channel management.

  1. Distribution and Supply Chain Management: Managing global supply chains to ensure efficient distribution of pharmaceutical products across different regions and countries. This involves logistics, inventory management, cold chain logistics (for temperature-sensitive products), and compliance with international trade regulations.

  1. Medical Affairs: Providing scientific and medical support for pharmaceutical products, including clinical research, medical education, scientific publications, regulatory interactions, and post-market surveillance activities.


Quality, not quantity

We have made quality of our habit. It’s not something that we just strive for – we live by this principle every day.


Quality, not quantity

  1. Patient Access Programs: Offering patient support services such as patient assistance programs, access to medicines, reimbursement support, patient education, and advocacy initiatives to improve patient outcomes and access to treatments globally.

  2. Licensing and Partnerships: Forming strategic alliances, licensing agreements, collaborations, and partnerships with other pharmaceutical companies, biotech firms, academic institutions, and research organizations worldwide to expand product portfolios, access new technologies, and enter new markets.

  3. Post-Marketing Surveillance and Pharmacovigilance: Monitoring the safety and effectiveness of pharmaceutical products after they are marketed, collecting and analyzing real-world data, reporting adverse events, conducting post-marketing studies, and updating product labeling or recommendations based on new information.

  4. Global Expansion and Market Access: Developing strategies for entering new markets, navigating international regulations, obtaining pricing and reimbursement approvals, conducting market research, and adapting products to meet the needs of diverse populations worldwide.

  5. Health Economics and Outcomes Research (HEOR): Conducting studies to evaluate the economic value, cost-effectiveness, and real-world outcomes of pharmaceutical products, including comparative effectiveness research, health technology assessments, and value-based pricing strategies.