Study Medication & Clinical Trial Support at Basic Pharma
Basic Pharma is dedicated to the development and production of study medication for clinical trials. As a trusted CDMO, we provide end-to-end support - from CMC (Chemistry, Manufacturing & Controls) and regulatory compliance to the manufacturing of investigational medicinal products (IMPs).
Our facilities enable the production of a wide range of dosage forms, including injections, creams, capsules, and hydrogels, all meeting the highest quality standards.
Partner with Basic Pharma to ensure your investigational products move efficiently from development to clinical trials.
Driving your Clinical Development Forward
As clinical programs progress and production demands increase, we support clients through every stage of scale‑up to ensure manufacturing processes evolve in a controlled and efficient way. Our team assesses process parameters, identifies scale‑dependent risks, and optimizes critical steps to maintain consistent product quality while enabling smooth transitions to larger batch sizes.
At Basic Pharma, the client is always central. Each partner works with a dedicated project team that coordinates activities, monitors progress, and ensures transparent communication. By understanding the needs of each formulation and development program, we provide practical solutions and proactive guidance. Our integrated expertise ensures a reliable, efficient path from early development to clinical delivery.
(Aseptic) Fill and Finish Capabilities
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Solutions
We process sterile and non‑sterile liquid formulations in controlled environments designed to safeguard product quality and consistency. Solutions can be filled into vials or prefilled syringes (PFS), depending on the needs of the study and the characteristics of the formulation. Where appropriate, we work with clients to evaluate alternative filling options that support project success.
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Powders
Powder formulations are handled in carefully controlled conditions to maintain accuracy, homogeneity, and stability. They can be filled into vials in quantities that meet the requirements for reconstitution or direct clinical use. If a formulation requires a specialized handling or an alternative packaging approach, we collaborate closely with clients to identify suitable options.
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Gels, Creams and Ointments
Semi‑solid formulations are filled under controlled conditions to ensure product integrity, texture consistency, and precise quantities. We offer filling into standard tubes and syringes and can jointly explore alternative solutions with clients when a formulation benefits from a different type of presentation.
IMPD Expertise in Primary Containers
Basic Pharma develops and manufactures Investigational Medicinal Products (IMPs) under strict GMP conditions, ensuring the safety, consistency, and reproducibility required for clinical use. Our team offers guidance throughout the development pathway, from small‑scale feasibility assessments to fully scaled clinical batches. With experience across a wide variety of liquid, semi‑solid, and capsule formulations, we help determine the optimal processing approach and support you through every stage of scale‑up and technical development.
Clinical Trial Packaging & Randomization
Our packaging, labeling, and randomization services are designed to meet the specific needs of clinical studies, including complex designs such as multi‑arm or double‑blind setups. We ensure that every product is packaged and labeled with precision, following clear regulatory expectations and maintaining full traceability across all steps. Randomization and blinding are carried out with the utmost care to secure study integrity, while our packaging processes support practical handling at trial sites and consistent presentation to patients.
GMP Manufacturing
PAH for Accurate Renal Diagnostics
Our diagnostic agent Sodium 4‑Aminohippurate (PAH) 2 g / 10ml provides a reliable and accurate tool for measuring effective renal plasma flow (ERPF). Produced under strict GMP standards, it is available on request to support medical research protocols that require precise and consistent kidney function assessment.
Services and Collaboration
We support your aseptic processing and filling of study medication for clinical trials. Looking for a reliable CDMO to support your clinical trial or product launch? Get in touch!