Pharmalytic
– Our Services
Analytical Services
Pharmalytic offers an efficient, accurate and reliable package
of analytical services for the pharmaceutical industry. Our detailed
understanding of analytical requirements allows us to support your
product development and marketed product activities.
The extensive range of our capabilities includes full ICH stability
and storage facilities, physical testing, raw material, API and
excipient analysis, inhalation studies and particle size analysis,
as well as method development and validation projects.
Our expertise and flexible approach at Pharmalytic facilitates
both client specific methodologies and bespoke project requests.
Our experienced analysts use state-of-the-art instrumentation to
complement traditional wet chemistry, in order to deliver every
project to you on time.
- Stability Testing
- Inhalation Device Testing
- Method Development & Validation
- Raw Material & QC Testing
- Analytical Techniques
Regulatory Compliance
Pharmalytic has demonstrated through FDA, MHRA and client inspections
that activities implemented within our quality system ensure our
service fulfils all quality requirements.
We conduct analysis for the Pharmaceutical industry in accordance
with the principles and guidelines of current Good Manufacturing
Practice (cGMP).
The effectiveness and applicability of our Quality Management system
is regularly monitored though self inspection procedures and quality
audits. Pharmalytic personnel also undergo periodic GMP training
to ensure the Company understands, and is adhering to, GMP requirements.
Other Services
In addition to our analytical capabilities, we are able to offer
full regulatory support and guidance to meet your requirements.
This can range from general consultancy to full programme management.
Our Project Managers work closely with our customers to ensure that
their analytical projects are designed and implemented in an efficient
and cost effective manner.
- Project Management
- Bespoke Projects
- Facilities
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