Our Best Services
Pharmaceutical development includes (but is
not limited to) formulation, such as API,
reformulation, screening, etc; preclinical
development, such as pharmacology services,
ADME-Tox, biomarker testing, and more.
Our Services include analytical testing
services, such as method development/validation,
bioanalytical testing, assay development,
clinical trials services, raw material testing
services, etc.; and contract pharma services,
such as CRO services/outsourcing, contract
packaging, contract manufacturing, etc.
We Aim To Make a Change In Our Community
Our dedication to quality in everything we do is uncompromising, and covers every stage of the development, production and marketing of our medicines: from the supply of materials through manufacturing and approval by the strictest authorities in the world..
Formulation development
Our many years of experience developing a breadth of formulations across a range of indications. Our innovative approach to formulation development integrates drug product development with clinical evaluation, combined with our experience with over 1,000 molecules at all stages of drug development.
We provides powerful formulation development services to support the development of many chemical substances. Our experts are fully aware of the importance of developing stable and compliant formulations to help customers find the right API and the best dosage forms for pharmaceuticals. Our R & D team has extensive experience in formulation research and analysis, as well as in collaborative practice with global customers for formulation development and analytical support. Our goal is to help the testing of molecules speed through the early stages and prepare our customers for commercial success faster.
Clinical trial manufacturing
Understanding that early phase clinical testing is a pivotal milestone in the development of your drug product, Whitman offers a clinical trial manufacturing, testing and certification service designed to meet your individual requirements. Our innovative method of building integrated GMP and GCP programs provides you with a streamlined, flexible approach to drug product supply that reflects your clinical study design and timeline. We understand the time and cost pressures you face during early phase evaluation and work with you to ensure a rapid, seamless path from development to clinical trial supply.
We understand your need to move rapidly through clinical development and have built the capability to efficiently scale up drug product manufacturing processes to meet the demands of global clinical and patient supply requirements.
Personal care
We have been providing personal care services to our local community since years back. Our goal is to deliver the most compassionate and most safety and quality which are vital for the manufacture of personal care products such as cosmetics, hair and skin care products and toiletries. End consumers are increasingly demanding proof of quality, compliance and efficacy from raw materials to finished products.
Household care products such as cleaning products and detergents are subject to the same close scrutiny. Our experts will help you demonstrate that your materials and products are compliant to market requirements, enabling you to trade all over the world with confidence.
Raw Materials
Any starting material intended for use in the production of medicinal products must be tested for identity, purity and quality. All deliveries of each batch of material must be sampled, tested and the results evaluated prior to manufacturing.
As the identity, purity and quality of a complete
batch of material is concluded from a small fraction
of the batch, sampling is an important operation.
Negotiating the dilemma of how much to take, how
many containers and the number of samples that may
be blended to form a composite sample, while
assuring that samples taken are representative of
the whole batch relies on sound statistical and
validation practices. This is for
Patient safety
To prevent costly manufacturing problems
Comply with Marketing Authorisation (MA) / Drug
Master File (DMF).