Formulation Development

R & D of conventional dosage forms, emulsions, microparticles, nanoparticles and related
testings (analytical and efficacy based)
Re8 facilitates formulation R & D, focusing on generic and low water-soluble substances. We have a strong network of reliable development partners for a variety of dosage forms like solid, semi-solid and liquid dosage forms.

Re8 ensures you have the right partner for your formulation challenges who offers innovative technologies and helps you scale up processes and products.

Our specialized partner makes sure you get customized nanoparticles and microparticle (lipid/ polymeric) products developed as per current regulatory guidelines. Other related services like analytical, stability, technology transfer, ex-vivo, and preclinical studies are accessible under one umbrella

Routes of Administration

Enteral
Parenteral
Topical

Our Expertise

Nanosuspension

Polymeric Nanoparticle

Sustained & Extended Rel Nanoparticles

Solid Lipid Nanoparticles

Nano & Micro Emulsions

Dendrimers

Tablets-capsules

Power-Granules

Gels

  • In vitro testing
  • Stability studies
  • Packaging development
  • Process optimization through QbD (ICH Q8)
  • Process validation
  • Manufacture of clinical batch
  • Tech transfer – process
  • Tech transfer–related analytical methods
  • cGMP Clinical batch production

Before developing any formulation recipe, it is very important to understand the drug and excipients used for better physicochemical stability and in-vivo performance.
The labs are equipped to evaluate solubility, pH, compatibility and related properties to ensure the development of a stable, robust formulation for you.

Once we understand your formulation goals, we will study thoroughly the solubility and compatibility profiles of API for optimal formulation development. With insights like the tentative market and expected performance in humans, we are able to design an ideal drug carrier for you. Accordingly, we design innovative recipe compositions, currently, we are active in OSDF, parenteral and dermal formulation development areas.

Re8 is happy to support you in the development of a proof-of-concept formulation that is a perfect product fit for the preclinical, clinical and commercial phases. 

Our team has a proven knowledge of effective product R & D and manufacturing process optimization. We optimize the prototype formulation for related stability and process development parameters to make your product commercially successful. Allow Re8 to be your first choice as a partner for formulation development and scale-up. 

Stability studies are key, to ensure a product is ready to enter certain geographical areas. We optimize the prototype formulation for related stability parameters to make your product commercially successful. Our certified storage chambers and analytical methods make sure you get a stable product as per ICH guidelines. 

We provide services to companies worldwide, faster, flexible and customized.
Share with us what you are looking for

Intellectual Property

IP rights stays with you, although we contribute to your success.
You remain sole owner of IP rights.

Your Ideas

Our Flexibility

Scroll to top

You cannot copy content of this page