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Liberty Pharma Inc.

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Liberty, Missouri, US

About Liberty Pharma Inc.

LPI is Audited by FDA December 2016 and we are pleased and proud to accept commercial samples. We are expanding our operations to 3 times.

Liberty Pharma INC. is an independent testing laboratory providing personalized product development and analytical services to the pharmaceutical (human and Veterinary)... Show more »

LPI is Audited by FDA December 2016 and we are pleased and proud to accept commercial samples. We are expanding our operations to 3 times.

Liberty Pharma INC. is an independent testing laboratory providing personalized product development and analytical services to the pharmaceutical (human and Veterinary) and chemical industries. We specialize in Product Development, Analytical Research and Development Testing Services, Quality Control Testing and Stability Storage & Testing Services

Liberty Pharma INC. is a DEA licensed testing laboratory with capabilities to handle Schedule I, Ia, II, IIa, III, IV, V Controlled substances, intermediates and drug products.

Liberty Pharma INC. was founded in 2014 to provide prompt and responsible Pharmaceutical services with integrity and uncompromising devotion to quality and client's confidentiality. Embedded with strengths of science, technology and acumen, Liberty Pharma INC. focuses on delivering quick turnaround of testing results with client’s methods and/or any compendia monographs with quality, compliance and turnaround time.

Testing services offered associated with the below instrumentation techniques with comprehensive and competitive turnaround time:

  • HPLC (UV and DAD detectors) – Assay, Impurities, Related substances, Residual solvents
  • GC – Residual solvents <467> and/or in-house methods, related substances, Assay
  • Dissolution – Single time point and profile of products
  • FTIR – Identification, Assay, product development
  • UV – ID, Assay, Dissolution analysis
  • Water/Moisture analysis - Karl Fischer, Halogen lamp
  • Heavy metals – USP - Method I, II, III
  • Sulfated Ash – EP and USP
  • Loss on Drying – USP and EP (Vacuum and Binder Ovens)

Our areas of Focus and expertise we offer our services but are not limited to:

  • Method Development and troubleshooting
  • Method Validation/Verification (Compendial and Non-Compendial)
  • Compatibility studies and stability studies
  • Forced Degradation studies (Stability-Indicating Method Validation)
  • Photostability analysis
  • De-formulation and reverse engineering of Reference Drug

Some of the areas of experienced and established services:

  • In-Vitro Bio-analytical/Bio-equivalence studies
  • Dissolution media studies
  • Simulated media studies (FaSSIF – Fasted State Simulated Intestinal Fluid, FeSSIF - Fed State Simulated Intestinal Fluid, FaSSGF – Fasted State Simulated Gastric Fluid, FeSSGF – Fed State Simulated Gastric Fluid)

Our goal is to provide high quality, cost effective and timely service, personalized to meet your needs.

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Diversity Certificates

Small business

Our Services (34)


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Particle Size Distribution

Price on request

WET and DRY

WET and DRY

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Residue On Ignition (ROI) Testing

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Density Measurement

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Chemical Deformulation and Reformulation

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Photostability Studies

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Forced Degradation Studies

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Stability-Indicating Method Validation

Stability-Indicating Method Validation

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Product Stability Testing

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Compendial Testing

Price on request

Compendial and Non-Compendial

Compendial and Non-Compendial

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Sulfated Ash Test

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EP and USP

EP and USP

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USP Water Testing

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Karl Fischer Titration

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FT-IR

Fourier transform infrared spectroscopy
Price on request

Identification, Assay, product development

Identification, Assay, product development

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Solubility and Dissolution Testing

Price on request

Single time point and profile of products

Single time point and profile of products

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Gas Chromatography (GC)

Gas Chromatography
Price on request

Residual solvents <467> and/or in-house methods, related substances, Assay

Residual solvents <467> and/or in-house methods, related substances, Assay

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HPLC

High Performance Liquid Chromatography
Price on request

HPLC (UV and DAD detectors) – Assay, Impurities, Related substances, Residual solvents

HPLC (UV and DAD detectors) – Assay, Impurities, Related substances, Residual solvents

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Pharmaceutical Product Testing

Price on request

All commercial pharmaceutical (human and veterinary) products can be sent to LPI... we are Audited by FDA and are in compliance.

Compendial and Non-Compendial

All commercial pharmaceutical (human and veterinary) products can be sent to LPI... we are Audited by FDA and are in compliance.

Compendial and Non-Compendial

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Mass and Weight Analysis

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Infrared Spectroscopy Services

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Assay Development

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Engineering and Fabrication

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Project Management

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Spectroscopy

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Product Development, Testing, and Packaging

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Liquid Chromatography (LC)

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Formulation Services

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Chromatography

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Strength Analysis

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Chemistry and Materials

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Separation/Purification Services

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Analytical Chemistry Services

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Material Testing Services

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Product Testing Services

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Imaging & Spectroscopy

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Physical Analysis Methods

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Harish Gosike

Director

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