Pharmaceutical and formulation laboratory

Method development

We can determine concentrations of active constituents and preservatives in almost any type of medicinal or agrochemical formulation.  We routinely develop, validate and document stability indicating assays using our in-house protocols that comply with the most stringent regulatory standards.

Our formulation laboratory is equipped with instrumentation for determination of physical parameters for liquids, solid and semi-solid dose forms.

Stability testing

Pia Pharma can manage your most complex stability projects, applying current knowledge of regulatory requirements to produce well-designed studies.  We scale-up development formulations and produce stability batches in our GMP licenced facility with short lead times.  A full suite of calibrated temperature and humidity incubators is available for long-term storage.  Our lab and regulatory teams work closely to produce stability reports and Chemistry dossiers to a high regulatory standard.

Quality control testing

We cater for your post-authorisation analytical needs with a full suite of contract analytical services available in our GMP licenced laboratory.  We’re setting the benchmark for this service, committed to meeting your expectations for quality, affordability, turn-around and communication.

Our aim is to reduce time to market, affording you minimum delay when waiting for quality control assay data. Samples are managed with our Laboratory Information Management System (LIMS) which reduces sample management and reporting times. With your specifications in our LIMS we can rapidly determine and report non-conformances. We strive to provide an efficient service that can save your business money and time.

We’re committed to meeting your expectations for quality, affordability, and turn-around

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