Unlocking a healthy future together
We are a globally respected CDMO motivated by a commitment to helping our partners create a healthier future.
Developing, Manufacturing & Marketing of Therapeutic Goods
We strive to go beyond what is expected, to deliver quality solutions and valuable partnerships.
Rely on us for integrated CDMO services to bring your concept to reality.
Great Ideas &
Life Changing Products
Our service offering includes new drug development, early stage formulation and analytical development.
Following early stage development, we continue with further development, scale-up and process validation ahead of commercial launch for a variety of dosage forms, all supported by full in-house analytical development and release laboratory.
Sypharma is
about People
At Sypharma we aspire to lead the way, unlocking opportunities and realising the full potential in every moment and every person. This gives meaning to everything we do and it is behind our focus and dedication.
By effectively working together in close collaboration our team tap into our full potential and drive every projects success
Quality & Compliance
Our uncompromising commitment to quality and compliance begins with research and development and continues through each stage of the drug development and commercialization process.
Unlocking potential at every stage
Sypharma is devoted to the development of new medicines and products that provide meaningful therapeutic benefit globally. Combining our extensive knowledge on a broad range of technologies, scientific rigor and creativity, our scientists, engineers and projects leaders use their expertise to deliver innovative and effective biotech solutions that make a difference.

DISCOVERY & DEVELOPMENT
Drug discovery process
Molecule Screening
PRECLINICAL RESEARCH
Formulation development and optimizationAnimal and
Toxicological Study
CLINICAL
TRIALSManufacture of GMP lots for clinical supply.
Phases I, II & III
REGULATORY SUBMISSION
Approval submission to regulatory authorities.Registration and
Market Authorization
COMMERCIAL MANUFACTURING
Cost-effective production & manufacturing capability.
Commercialization

Quality our clients and collaborators rely on
We are proud to hold accreditation across international codes of Good Manufacturing Practice (GMP) and all our goods and services are supplied under license of the Therapeutic Goods Administration (TGA), ISO13485 Medical Device and the Australian Pesticides and Veterinary Medicines Authority (APVMA).
















