Formulation Development Service in Thane (फॉर्मूलेशन डेवलपमेंट सर्विस, ठाणे)

Personal Care, Home Care and Colour Cosmetics. Food Beverages. Formulation Research on Raw Materials. Cosmeceuticals. Neutraceuticals. Personal care, Home care, Natural and Organic and Colour cosmetics.

Company s performance edge is based on offering Quality-By-Design (QbD) concepts at all stages of formulation development. The Design of Experiments (DOE) along with relevant time scale and risk assessment helps us to develop the strategy for further experimentation.

Formulation Development

Formulation Development Service

Pharmaceutical Formulation R & D

Formulations Facilities

Custom Formulation Development

Formulation development services

Prototype Formulation Development

Formulation Development Service

Contract Formulation Development

Formulation Development Service

Formulation Development Service

Formulation Research and Development in Cipla is accomplished by experienced scientists, technicians and chemists. The team specializes in creating alternate and patentable processes for generic formulations. It is equipped to conduct the following processes for formulation development: Product and process optimization Analytical method development Analytical method validation Evaluation and techno-marketing studies Technology transfer

Our Research Formulation team is dedicated to continuous innovation and staying abreast of the latest advancements in the beauty industry. Whether you have a specific ingredient in mind or need assistance with product development, we offer expert guidance and expertise to create effective and cutting-edge cosmetic formulations.

We offer a range of pre-formulation and formulation development services on new active substances, generics and upgrades of existing formulations.

Formulation Development Service

FORMULATION AND DEVELOPMENT

Formulation Research Development Service

as a logical extension of our current engagement in clinical research and with an objective to emerge as the complete partner in drug development process, in august 2006, we forayed into formulations development activity. A total area of 30000 sq ft has been earmarked for this activity. 1st phase spread over an area of 3500 sq ft is fully operational and the 2nd phase would be completed by december 2007. by integrating various services under one roof, we are aiming to provide a complete resource that enables our clients to progress from pre-formulation to clinical trial quickly, safely and cost-efficiently. with management cutting back on r d resources, we understand the intense need to create optimal formulations under tight timelines with a limited amount of api. And therefore any formulation development project that is undertaken starts with a thorough analysis of the preformulation data report, the intended manufacturing process, any patient compliance issues and the strategic goals of the sponsor company. our logical, data-driven approach to formulation development gives the compound the best chance at success and provides our clients the most efficient, straightforward process for manufacturing the compound. our formulation development team undertakes work on new active substances, generics and reformulation of existing products. Our facility with class 100,000 gmp area and conforming to cgmp offers following services: pre- formulation formulation of wide variety of dosage forms analytical method development validation stability studies as per ich guidelines product development report documentation in ctd format process validation and technology transfer preparation of dmf / cos

At SDS Laboratory we recognize the importance of our clients requirements to develop robust formulations and advancing optimal dosage forms. Our goal is to help our clients minimize development problems, costs and timelines. Working with our clients we offer and evaluate the following parameters when developing and manufacturing certain dosage forms for APIs.

Formulation development Analytical method development and validation Stability evaluation and analysis as per ICH guidelines In-vitro equivalence and Dissolution studies Process validation Technology transfer API source evaluation Preparation, Compilation and Submission of reports in CTD/eCTD format

This outlined approach to pre-formulation and formulation development result in significant saving to the client by eliminating the variables associated with suboptimal formulations using QBD approach.Preclinical development efforts in PK and PD occur with confidence which eliminates inclusion of additional uncontrolled variables from unstable formulations into the study. 1) Solid oral dosage formulations (Granules/ pellets, capsules/ tablets for immediate release or modified release).2) Liquid oral formulations (Syrups and suspensions)3) Topical and semi solid formulations (Creams, gels etc.)

Formulation Development Services: Product Development at VivaTest begins with Patent Landscaping and Strategy Development. Desired product attributes are identified and prototype formulations are developed to meet the desired product attributes. Critical process parameters are identified and process optimization studies are carried out. Based on the formula and process optimization studies, final composition and manufacturing process is recommended for bio-study and scale-up. VivaTest offers Formulation Development Services across diverse Dosage forms such as Oral Solids, Oral Liquids, Disperse Systems, Semi- Solid preparations, Ophthalmic Drug Products and Nasal Systems. VivaTest has a state of the art facility meeting International Standards and Regulations. The Analytical Laboratory is GLP compliant and the Formulation Development Laboratory is GMP compliant with perfect in-built systems.