ManufacturingCapabilities

MANUFACTURING ABILITIES

HPPE focuses on the development and manufacture of a variety of specialty chemical and biological products. We
are an FDA registered facility that specializes in the production and processing of active pharmaceutical
ingredients and various excipients under GMP guidelines.

Our manufacturing facility includes:
Large capacity processing vessels (200 – 13,000 gallon)
2000 sq ft Class 1000 clean room cGMP
Dedicated GMP laboratory (1kg – 100kg)

Clean room facility includes:
High security access with fingerprint recognition
Large capacity automated sterilizer
In-line processing tanks with agitation
Ion-exchange chromatography for endotoxin removal
Chromatographic systems with a range of functionality
Filtration systems with custom processing capabilities
High throughput atomizing spray dryer for powder processing

                           Clean room floor space                                                                                   Spray Dryer

GMP Laboratory
HPPE has a dedicated GMP laboratory with capability of manufacturing APIs and excipients for batch sizes
1 – 100 kg.
Laboratory equipment and facility is cleaned and sanitized before and after batching.
All consumables, starting materials and intermediates are removed post production.

Quality Control Laboratory

                                                        (Analytical Capabilities)

USP Purified Water System
The purified water quality meets USP standards and is used
throughout the facility in the manufacture and processing of APIs and
excipients.

                                 Reverse Osmosis System


                                                                                                                                                         Water System (floor length)