Contract Research

Syngene International Ltd. provides wide range of services which includes prep hplc, It belongs to process R&D and cGMP manufacturing services category. Contact us for more information.

Syngene’s Oligonucleotide capacity & services ranges from development to cGMP manufacturing of chemically synthesized high quality modified and non-modified custom Oligonucleotide (DNA/RNA), siRNA (single & double stranded, miRNA (modified and non-modified), Antisense, fast delivery of Oligonucleot...

Actylis offers GMP, biopharma and non-GMP specialty chemical custom ingredient research and development services by generating robust, practical and cost-effective processes for the preparation of specialty chemicals, excipients, and pharmaceutical ingredients. With decades of experienc...

Cell-based bioassays that comply with cGMP: Using a variety of techniques, including cell-based assays, ligand and receptor binding assays, and flexible multiple assay approaches – our potency testing experts offer tailored bioassay method development, method transfer and method validation to ICH Q2 (R1)...

Solvias provides high calibre microbiology, chemistry, toxicology and cell biology services according to GMP, CGMP (FDA), GLP and ISO 17025 standards.Testing for sterile and non-sterile products / Environmental testing / Specialised studies (antibiotics, integrity testing, alternative methods) / Endoxin an...

NUVISAN has over 40 years of experience providing clinical trial supplies services, offering a comprehensive range of solutions. These solutions include regulatory consultancy, manufacturing services, packaging and labeling, randomization list creation, analytical testing, just-in-time labeling and distrib...

PI Health Sciences is your strategic partner in cutting-edge CRO Services. We specialize in core chemical discoveries, synthesis, analytical research, and more. Trusted by global pharmaceutical giants, we prioritize quality, IP protection, and data security. Our expertise spans from drug discovery to comme...

1) Analytical Testing Of Pharmaceuticals & Cosmetics2) Biotechnological Services
3) Microbiological Services
4) Bio - Compatibility Studies of Medical Devices(As per ISO 10993USFDA and MHLW Guideline)
5) Preclinical & Toxicological Services
6) Phytochemical & AYUSH Testing Se...

ACDIMA BioCenter is a comprehensive clinical CRO based in Jordan and founded in 2000. ACDIMA BioCenter is a multinational investment operates as business-driven mode with focus on supporting the industry of clinical trials and bioequivalence studies services that help expediting their regulatory approv...

For pharmaceutical, biotech, and medical device manufacturers, Quality Management Systems (QMS) are the foundation for enabling the organization to operate in a compliant manner. The QMS establishes the path to compliance for the company and enables sustainable systems that meet the demands of re...

To accelerate the development and marketing of your Biotherapeutics, Quality Assistance offers a complete analytical package to meet the EMA and FDA requirements, all on one site.

Whether it is to extend your analytical capacities or to outsource parts or all of your analytical needs, ...

We are a Full service CRO with EMA / ISP CHILE / DCGI / CDSCO Compliant  clinical & Analytical Facility for conducting BA/BE studies.
• With 60 bedded  Clinical facility  & Bio- Analytical Facility for BA/BE Studies following strict Regulatory Guidelines Meeting  Internation...

Our team of experts would be delighted to share their knowledge and experience with you. These services could be both theoretical and practical, and located either in Solitek’s site in Barcelona or at the customer’s choice of venue. Please contact us for more information.

Accelerated drug development through interdisciplinary integration and expert coordination of all drug development activities “under one roof”
Industry-leading timeline from candidate nomination to regulatory submission
Custom-designed, flexible development plans allow for real-time adjustments a...

ADAPTEK® TECHNOLOGY is the general name for our 4 international patents and expertise in nanotechnology and controlled release systems.This is a transversal technology that allows to develop customized biopolymeric nanohydrogels, allowing the load with different API (drugs, vitamins, growth factors, etc.)....

All Pharmaceutical Reference Standards are supplied with Certified COA along with supporting analytical data like HPLC, Mass, NMR, CMR, UV, IR, TGA, ROI, CHNS.

Excipients can have an important impact on the manufacturability and pharmaceutical performance of a formulation. It’s therefore important to identify and control functionality related characteristics (FRCs) of excipient materials in order to achieve safe, robust and stable products. Expe...

We are world's leading contract manufacturer.  

The use of oligonucleotides is rising for the diagnosis and treatment of illnesses. Cutting edge research often requires complex oligonucleotides, the synthesis of which requires a deep understanding of nucleic acid chemistry. Our experienced scientists can synthesize complex oligonucleotides for your imme...

Functional Invitro Human based organ on chip to assess safety pharmacology.