As part of its overall mission,
PTI can provide a wide range of services that are designed to compliment its
clients' internal development capabilities and help to reduce both cycle times
and costs associated with the development process.
PTI also offers global regulatory
inspection services, and training programs in the area of solid dosage
formulation and processes.
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PTI's laboratory capabilities
enable fundamental material data (which are critical to the overall
dosage-form development process for oral dosage forms) on active drug
substance and excipients to be established.
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As a companion services to its
Preformulation Services, PTI can generate State-Of-The-Art Compaction
Simulator Aided tabletability (compaction) profile on the client's individual
raw materials (both drug substances and excipients) and formulations.
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PTI can provide both consultative
services in support of the formulation development process, as well as
undertake active laboratory projects on behalf of clients to develop prototype
formulations for oral dosage forms (immediate release and modified release).
In addition, this development process can be expanded to include the design of
the formulations that are either ready for scale-up, or that have been
subjected to such a process.
Critical analytical support, such
as developing appropriate analytical methods and undertaking initial stability
studies, can also be accommodated. |
For further information,
please click on
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For further information,
please click on
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PTI team members are involved in
global pharmaceutical consulting and have been hired many times to provide
expert witnessing services because of their extensive knowledge on
pharmaceutical dosage form development related issues. For further
information on a variety
of services, such as PROCESS DEVELOPMENT, TECHNOLOGY TRANSFER, REGULATORY
AFFAIRS please contact us:
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