Priosh

At Priosh PharmaChem AG, we offer a comprehensive suite of pharmaceutical services that drive innovation and ensure exceptional results. From drug discovery, formulation development, clinical research to GMP material and API manufacturing, we cover every phase of the pharmaceutical development lifecycle with precision and dedication.

Research and Development

Empowering Breakthroughs from Molecule to Medicine

Our R&D services are built on a foundation of deep expertise and cutting-edge technology, transforming bold ideas into actionable results. We focus on developing innovative solutions for complex pharmaceutical challenges through tailored approaches in medicinal and synthetic chemistry.

Clinical Research Services

Ensuring Smooth Operations at Every Stage

Through our clinical research organisation (CRO) services and preferred site management organisation (SMO) partnerships, we take the burden off your shoulders by managing every detail of your clinical trials. With strong expertise in cardiovascular, CNS, and oncology research, as well as other therapeutic areas, and leveraging the latest AI technology, Priosh ensures your trials are run smoothly, cost-effectively and in compliance with the highest regulatory standards.

API Manufacturing

Your Premier Partner for High-quality APIs

At Priosh, API manufacturing is more than a process; it’s a commitment to excellence. Our facilities are designed for efficiency, ensuring seamless transitions from chemical synthesis to product delivery. We adhere to the highest global standards, providing cost-effective and reliable solutions tailored to your exact needs. Whether you're looking for flexibility, scalability, or the assurance of consistent quality, Priosh delivers the right ingredients to bring your vision to life.

  • Small Scale API Production: Critical for discovery & development under non-GMP conditions.
  • Scale-up Capabilities: From grams to metric tons with c-GMP manufacturing.
  • Custom Synthesis: From milligram (mg) quantities to several kilograms (kgs).

We offer a comprehensive range of equipment and capabilities for various scales of production, including large-scale hydrogenation, cryogenic reactions, and chiral synthesis.

Drug Discovery

Discover the Future of Medicine

At Priosh, we are unlocking the future of healthcare with our cutting-edge drug discovery services. Combining synthetic and medicinal chemistry with the latest technological advancements, we transform ideas into revolutionary treatments. Our experts collaborate with you from concept to creation, leveraging deep industry knowledge to uncover compounds with the potential to redefine healthcare.
Every molecule we design represents a new opportunity for innovation, a new step towards changing lives.

Our solutions include

  • Route Design
  • Custom Synthesis
  • Parallel Synthesis
  • Library Design and Synthesis
  • Complex Chemistries: Including phthalocyanines, polysaccharides, peptides and challenging reactions

Our chemical process R&D team, composed of scientists that excel in challenging projects, including rapid route scouting and process optimization for scale-up.

We offer

  • FTEs (Full-Time Equivalent)
  • FFS (Fee for Service)
  • Risk Sharing

Our scale-up capabilities extend from non-GMP to c-GMP manufacturing, handling projects from grams to metric tons without the need for technology transfer. We also offer kilo-scale laboratories equipped for various processes.

Formulation Development

Turning Ideas into Life-changing Therapies

When innovation meets precision, formulations come to life. Priosh's formulation development services ensure that your pharmaceutical products are scientifically sound and market-ready. From pre-formulation studies to advanced product development, we design medicines that are not only effective but revolutionary.
With Priosh, every formulation is a step toward creating solutions that make a real difference in patients’ lives - affordable, impactful, and globally accessible

Pre-formulation Studies

  • API Characterization: Solubility studies, particle size, polymorphism, bulk properties, hygroscopicity, photostability studies, intrinsic stability studies
  • Drug-excipient Compatibility Studies
  • Selection of Appropriate Packaging Material

Formulation Capabilities

  • Oral Solids: Immediate release tablets and capsules, modified release tablets and capsules (delayed release, extended release, targeted release), bilayer tablets, fixed-dose combinations
  • Oral Liquids: Solutions and suspensions
  • Injectables: Simple injectables, aqueous and non-aqueous solutions, lyophilized injections, complex injectables (liposomes, nanoparticles, microemulsions)
  • Peptides/Polypeptides/Proteins

We follow ‘Quality by Design’ principles in drug product development, offering analytical capabilities including routine analysis, method development and validation, stability studies, and technology transfer.

Clinical Research

Setting New Standards in Clinical Excellence

Priosh through its CRO services capabilities and preferred SMO partnerships, leads the way in clinical research for all therapeutic areas, particularly in oncology, CNS, and cardiovascular. We provide a strategic approach to clinical development for conducting rapid and cost-effective trials through leveraging the latest AI technology facilitating comprehensive trial management across all phases of clinical trials, including NCE, biosimilars, BA/BE, NIS, interventional and observational studies.

Priosh offers a full range of clinical development services, from early phase planning and regulatory strategy, study setup and start-up, and clinical operations and study conduct, to data handling, analysis, and reporting, as well as all aspects of drug safety across all study phases, including post-marketing surveillance trials. Based on the needs of your project, the services can be contracted as a full-service, end-to-end solution or as functional single-service solutions.

Our rigorous trials guarantee that every product is safe, effective, and meets the highest regulatory standards. We don't just run trials; we set new standards in precision, safety, and results - moving science forward for a healthier tomorrow.

Our Services Cover the Full Spectrum of:

  • Strategic Consulting
  • Clinical Development Planning
  • Project Management
  • Regulatory and Study Start-up
  • Clinical Monitoring
  • Drug Safety and Pharmacovigilance
  • Data Management and Biostatistics
  • Medical Writing
  • Quality and Compliance
  • Medical Monitoring

We enlist therapeutic and regulatory experts to build a customized strategy to meet your goals and select the best path forward.

We offer a collaborative partnership with a network of experienced investigators and research for multicenter trials, ensuring diverse patient populations and comprehensive data.
As your partner of choice, we become an integral part of your team from the moment of contract award to the delivery of the clinical study, with a core mindset focused on delivering on time, within budget, and with the highest quality.

Oncological Biorepository

Preserving the Future of Cancer Research

Our Oncological Biorepository is more than a storage facility - it’s a foundation for breakthrough oncology research. We meticulously collect and preserve vital biospecimens such as blood and tissue samples, ensuring researchers have access to high-quality samples for developing next-generation cancer treatments.

Priosh provides the critical building blocks for the future of oncology, safeguarding today’s research to secure tomorrow’s cures.

Our biorepository includes

  • Tumor/Adjacent Normal Tissue Samples:
    • RNA Later: Stabilizes RNA to prevent degradation.
    • Snap Frozen: Preserves cellular structure and biochemical integrity.
  • Biopsy Samples: Small tissue samples for molecular analysis.
  • Bodily Fluids: Includes serum, plasma, urine, and saliva.
  • FFPE Blocks: For long-term storage and histological analysis

Note: Sample collection is based on feasibility and is not compulsory.
All samples are collected with strict adherence to ethical standards, ensuring patient privacy and consent. Our advanced storage and traceability systems make these biospecimens easily accessible to researchers worldwide, accelerating breakthroughs in cancer diagnostics and treatment.