Azopharma Product Development Group
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Contact:
David Greeley
Chief Administrative Officer and VP Sales & Marketing
Phone #: 954-433-7480
Fax #: 954-432-9015
Email: development@azopharma.com
Website: www.azopdogroup.com |
Address:
Two Oakwood Boulevard, Ste. 170
Hollywood, FL 33020
United States of America
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Company Description:
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Azopharma Product Development Group provides full product development and stand-alone services for the pharmaceutical, biotech and medical device industries. From preclinical to late phase development projects, Azopharma provides total product development services. Our capabilities include: Full IND Development, Full NCE Development, Full ANDA Development, Full Medical Device Development. Please contact us to review your project requirements. |
Additional Information:
Azopharma Product Development Group deals in the following categories:
| Accelerated Stability Studies |
ADMET |
| Analytical Lab Services |
Analytical Methods Development |
| Analytical Validation Studies |
Assay Development |
| Auditing |
Bioanalytical Analysis LC/MS/MS |
| Bioavailability Studies |
Biological Testing |
| Chemical Analysis |
Chemistry, Combinatorial |
| Chiral Separations, R&D |
Chromatographic Analysis, LC/GC |
| Clean Room Services |
Clinical Analysis |
| Clinical Monitoring |
Clinical Supply Management |
| Clinical Trials Management |
Clinical Trials, Phase I |
| Clinical Trials, Phase II |
CMC (Chemistry, Manfacturing & Controls) |
| Consulting |
Consulting, Regulatory |
| Contaminant Analysis |
Contract Manufacturing |
| Custom Synthesis |
Dissolution Testing |
| Distribution, Clinical Trials |
Dosage Form Development |
| Drug Delivery Systems |
Drug Development Services |
| Drug Discovery Support Services |
Efficacy Testing |
| Endotoxin Testing & Removal |
Expert Testimony |
| Extractables / Leachables Testing |
Forced Degradation Studies |
| Formulation Development |
Formulation Services |
| GLP Auditing |
GMP Auditing |
| HPLC |
Immunotoxicity Testing |
| In Vitro Testing |
In Vivo Testing |
| IND/NDA Submissions |
Library Synthesis |
| Lot Release Testing |
Lyophilization |
| Manufacturing, API |
Manufacturing, Aseptic Fill/Finish |
| Manufacturing, Bioequivalence |
Manufacturing, Clinical Trials Supply |
| Manufacturing, Controlled Substances |
Manufacturing, Cytoxic & High Potency Compounds |
| Manufacturing, Dose Form, Non-Sterile |
Manufacturing, Dose Form, Sterile |
| Manufacturing, Ethical |
Manufacturing, High Containment Operations |
| Manufacturing, Oral Drug Delivery |
Manufacturing, Other |
| Manufacturing, Parenterals, Small Volume |
Manufacturing, Powders |
| Manufacturing, Semisolids |
Manufacturing, Solid Dosage |
| Manufacturing, Solutions & Suspensions |
Manufacturing, Sustained Release |
| Manufacturing, Tablets |
Manufacturing, Topicals |
| Mass Spectrometry |
Materials Analysis |
| Medical/Clinical Studies |
Metabolic Analysis |
| Methods Development |
Methods Validation |
| Micro FT-IR Analysis |
Microbiological Testing |
| Microscopic Analysis |
Nonclinical Research |
| Organic Synthesis |
Packaging, Clinical Trial Materials |
| Packaging, Clinical Trials |
Packaging, Development |
| Parenterals Development |
Particle Size Analysis |
| Particle Size Classification |
Pharmacokinetics |
| Pharmacology |
Photostability |
| Physical Testing |
Preclinical Study Design |
| Preclinical Testing |
Preclinical Testing Formulations |
| Preformulation |
Process Development/Scale-Up Services |
| Process R&D |
Process Validation Studies |
| QA/QC |
R&D Services |
| Raw Materials Analysis |
Stability Studies |
| Stability, ICH |
Statistical Analysis |
| Sterility Testing |
Storage |
| Sustained Release Delivery Systems |
Tablet Coating |
| Thermogravimetric Analysis |
Toxicology Services & Analysis |
| Trace Metal Analysis, ICP |
Transdermals |
| UV-VIS Spectrophotometer Analysis |
Wet Chemical Analysis |
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