- Service Details

By using microfluidization technology process, Skyepharma provides preformulation / micronization solution to increase bioavailabity of poorly soluble APIs. It is also an interesting technology for micro and nano emulsion manufacturing.

- Service Details

With expertise in characterizing and modifying a drug substances' physical, chemical and mechanical properties, our objective is to help you assess and choose the best solid form for progression into animal and human dosing trials.

- Service Details

By rapidly screening excipients and selecting appropriate formulations, you can begin preclinical studies in a matter of weeks rather than months.

- Service Details

To support API solid form R & D programs, we apply High-Throughput Screening Technology for discovery of new polymorphs, particle size engineering & development or automated crystallization scale-up development.

- Service Details

Our Pre-clinical & Phases I & II services include pre-formulation, formulation development, analytical method development & evaluation, cleaning residue test, CTM lots testing, analytical method development & validation etc.

- Service Details

The Formulation R & D Capability includes Design and development of new dosage forms, Pre formulation studies, Lab / pilot scale studies, Process optimization/validation studies, Stability studies as per ICH guidance, Technology transfer of new products.

- Service Details

Crenza is a full scale R&D centre for development of Parenteral and Ophthalmic drug products. Crenza is founded by Industry professionals with invaluable experience and proven track record of development and commercialization of Parenteral and Ophthalmic drug products for regulated markets.

- Service Details

Progenerics Pharma is focused on developing high quality affordable generic products for global markets. Facilities are capable of developing all dosage forms like General Solids and injectables, Oncology Solids and Injectables including Lyophilized products, Creams & Ointments, Hormones and

- Service Details

Appco Pharma functions with a goal to deliver product development solutions to its clients that help them enhance the ROI of their drug development portfolio.

- Service Details

AMRI's Process Analytical Technology (PAT) approach is consistent with the FDA perspective that quality cannot be tested into products, but should be built in.

- Service Details

We have extensive experience in the testing of drug products from preclinical development to commercial drug products including preclinical prototype evaluation, Excipient compatibility, physical characterization, ICH stability testing of drug products.

- Service Details

During the pre-formulation phase, Eurofins CDMO determines the physical & chemical properties of the API. Our team has experience with a wide range of different drug delivery routes, drug delivery systems and drug production technologies.

- Service Details

Preformulation concept studies to accelerate your drug development and approval.

- Service Details

Our dedicated team of scientists have their core training in the area of preformulation and have expertise in the complete pharmaceutical profiling of molecules.

- Service Details

During the pre-formulation phase, Eurofins CDMO determines the physical & chemical properties of the drug substance. In the formulation development phase, We assess different drug product concepts in terms of stability, efficacy & processability.

- Service Details

Early phase formulation development to accelerate your drug development and approval.

- Service Details

Formulation Development is the core activity at Zenvision Pharma and it includes Pre-formulation studies, formulation development, analytical method development & validation, stability studies, Dossier preparation & Technology Transfer.

- Service Details

We offer full service solutions and project management for cost effective product development in pharmaceutical as well as food /nutraceutical areas.

- Service Details

The R&D Department is staffed with fully trained and highly experienced scientists and has at its disposal state-of-the-art facilities striving to produce products according to GMP/GLP global standards.

- Service Details

Innovative, non-toxic and fully biodegradable biopolymers, made of hydrophilic (PEG or modified PEG) and lipophilic (PLA, PLGA, CPL) blocks.

- Service Details

Alternative to the use of inactivated viruses. Synthetic cationic polymers for nucleic acids (DNA or RNA) and hydrophobic APIs transfer.

- Service Details

2D or 3D biopolymers that generate biodegradable dendrimers used in cosmetics and to vectorize an API or a fluorescent probe.

- Service Details

Pre-formulation activities are one of the most crucial areas of the product development process. These activities determine which process and delivery methods will provide the most stable form of the drug.

- Service Details

We provide full range of analytical services, State-of-the-art instruments, cutting-edge technologies, and experienced scientific staff ensure efficient, high-quality and cost-effective services.

- Service Details

Crystallics has capabilities to determine powder properties like bulk and tap density, flow properties, odor & color, electrostatics, compression properties, compaction properties, milling, grinding & granulation (chemical physical stability).

- Service Details

Whether it is a New Chemical Entity or a mature API, Galenix can help with the characterization and the building up of the Drug Master File (DMF) which is deemed necessary for the final registration process.

- Service Details

Bluepharma currently has the capability for the development of potent drugs, from the initial steps of the development until the manufacturing of submission batches.