Pharmaceutical Development

We offer fully integrated pharmaceutical development and GMP manufacturing services across a wide range of sterile and non‑sterile dosage forms. Whether you are developing a nasal spray, pre‑filled syringe, cream, ointment, solution, or suspension, our multidisciplinary teams deliver the scientific, technical, and regulatory expertise needed to bring high‑quality products to market efficiently.

We support both generic and innovative drug products, offering a true end‑to‑end CDMO model, from early formulation design through commercial manufacturing.

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Scientific Expertise Across Formulations

Our development capabilities cover a broad portfolio of dosage forms and therapeutic categories.

  • Formulation development (solutions, suspensions, semi solids)
  • Device and primary packaging development (e.g. nasal pumps, syringes, tubes)
  • Analytical method development, transfer, and validation
  • Process development, optimization, and scale up
  • In-vitro performance testing and bioequivalence studies
  • Regulatory guidance throughout the lifecycle
  • GMP manufacturing for clinical and commercial phases
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Product Upscaling from Lab to Commercial Manufacturing

With robust, science‑driven scale‑up capabilities, we bridge the gap between laboratory development and commercial production. Drawing on extensive experience across diverse dosage forms, we ensure your product maintains quality, consistency, and performance while transitioning smoothly from early development to market‑ready manufacturing - minimizing risk, accelerating timelines, and enhancing manufacturability.

  • Scale‑Up & Process Translation

    We translate lab‑scale formulations into reproducible pilot‑scale batches, ensuring a smooth and predictable scale‑up. Our expertise focuses on identifying and managing scale‑dependent parameters to maintain process robustness across all development stages.

  • Process Control & Quality Consistency

    We safeguard product quality by controlling Critical Process Parameters (CPPs) and ensuring consistent Critical Quality Attributes (CQAs) at every scale. This guarantees reliable performance and supports data‑driven decision‑making throughout development.

  • Tech Transfer & Manufacturing Readiness

    From engineering batches to full GMP tech transfer, we prepare your process for commercial manufacturing. Our team supports validation activities and optimizes device‑filling workflows for pumps, syringes, tubes, and other delivery systems.

Proven Expertise

Nasal Delivery Systems

Over the years, strong expertise has been built in nasal drug delivery systems. This includes the development and manufacturing of both generic and innovative non‑pressurized nasal spray products, covering solutions and suspensions.

We have hands‑on experience with key APIs such as:

  • Xylometazoline
  • Mometasone Furoate
  • Fluticasone Propionate & Fluticasone Furoate
  • Azelastine combinations
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Flexible Development Models

Self- or Co-Developed Products

Strategic decision‑making is essential for successful pharmaceutical development, especially for complex generics. Our end‑to‑end development services de‑risk your program by identifying which studies are essential, which are justified, and where efficiencies can be gained. We support:

  • Your Own Molecule or Formulation
  • Full Co-Development Partnerships
  • Licensing Opportunities
  • Development for Global Markets
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Quality through Scientific Insight

Our development framework is built on a complete evaluation of all Critical Quality Attributes (CQAs), ensuring robust product performance, safety, and compliance across all dosage forms. We focus on:

  • Product Stability
  • Device-Product Compatibility
  • Microbiological Integrity
  • Dose-Delivery Consistency
  • Rheological and Physical Characterization
  • Impurity and Degradation Profiling
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Driving Your Program Forward with Confidence

From early development through commercial‑ready scale‑up, our team combines scientific rigor with practical manufacturing and regulatory insight to strengthen every stage of your pharmaceutial journey. Whether you’re advancing a complex generic or innovating a new formulation, we help you move forward with confidence. 

Ready to explore how we can support your project? Contact us today.