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)
Method Verification / Validation Program   
Gel Permeation Chromatography (GPC) with MALLS and DRi detection  
HPLC with PDA and Fluorescence detection
Rheometer
Gas Chromatography
UV-Vis Spectroscopy
Analytical Balances
Raman Spectroscopy
Potentiometric Titration
Furnaces and Ovens
Capillary and Dynamic Viscosity
Various Wet Instruments
Endotoxin Test Instruments
Stability Units
HPPE LLC │ 6906 Dixie St, Columbus, GA 31907 │Phone: 706- 563-9290, 706-563-9654 │ Fax: 706-563-0719 │ info@hppeco.com

Next Generation Biopolymers