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Solid Pharmaceutical Product Experts| The following experts are available as solid pharmaceutical product consultants and solid pharmaceutical product expert witnesses. Intota experts are peer-recommended authorities who have been carefully selected and rigorously screened. | |
| | Definition: Solid Pharmaceutical Product -
A pharmaceutical product in solid form, such as a tablet as compared to liquid cough syrup. |
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| 1 to 24
(of 24) | | | Solid Pharmaceutical Product Experts |
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Expert Quote | | |  | | Expert in Controlled-Release Drugs
Solid pharmaceutical product; tablet coating; drug dosage form development. Expert has served as Director of Product Development at the leading firm involved in the discovery and application of pharmaceutical coating products and technology. See full profile | | Pennsylvania (PA), USA  | | | |  | | Expert in Pharmaceutical Manufacturing, Research and Development, Education & Training
Expert's primary experience in tablet manufacturing covered conventional pharmaceutical tablets for a variety of drugs and chewable tablets of antibiotics, utilizing both dry and wet granulation techniques and a variety of processing and tablet ... See full profile | | Florida (FL), USA | | | |  | | Expert in Formulation, Development and Manufacturing of Pharmaceutical Dosage Forms
Expert has extensive product development experience in solid dosage forms (TABLETS {IR & ER} , HARD & SOFT GELATIN CAPSULES AND POWDERS); Liquid dosage forms ( SOLUTIONS, SUSPENSIONS & EMULSIONS) from conception through to stability trail, clinical ... See full profile | | NSW, Australia | | | |  | | Expert in Pharmaceutical Solid Dose Forms
He has worked in the development and manufacturing of chewable tablets either for the delivery of locally (oral) acting drugs with a variety of excipients and basic tableting technology and in the development of medicinal candy products enclosing vitamins ... See full profile | | Argentina | | | |  | | Expert in Chemical processing, powder processing, energetic materials, automotive safety, Aerospace/Defense
Expert has over 30 years experience in process development, pilot scale operation, scale-ups, process equipment selection, chemical processing and formulations development, designs and trouble shooting of chemical and solids processing plants. See full profile | | Michigan (MI), USA | | | |  | | Expert in Pharmaceutical Product Development, Dosage Forms, Controlled Release, QC/QA, GMP, China
Expert has worked in the pharmaceutical industry as a research scientist, QC/QA director, vice president of product development, and has been involved in product development from pre-clinical through Phase 1 production. Expert has experience in setting up ... See full profile | | Oklahoma (OK), USA | | | |  | | Expert in Pharmaceutical Product Development, Analytical Chemistry, Material Science, Process Development
Expert has extensive experience in pharmaceutical product development, particularly in developing drug/medical device combination products. He has over 15 years relevant experience in the pharmaceutical industry, highlighted by the launch of an anticipated ... See full profile | | California (CA), USA | | | |  | | Expert in Pharmaceutical Technology, Scale-up, Wet granulation end-point, Tableting, Compaction
Expert has 25 years experience in pharmaceutical process scale-up, wet granulation end-point determination, compaction and tableting. He has published many articles on these topics, edited "Pharmaceutical Process Scale-up" handbook, and wrote chapters ... See full profile | | New Jersey (NJ), USA | | | |  | | Expert in Regulatory Sub. NDS, ANDS, SANDS, NC, Cross References, Natural Health Products, Medical Devices
Expert's firm has extensive expertise in regulatory submission. They provide different regulatory strategies to their customer's and prepare all types of submissions on their behalf. Expert also has extensive expertise in Narcotic's regulations. See full profile | | Quebec, Canada | | | |  | | Expert in Europe Drug Market, Drug Reimbursement, Drug Therapy, Generic Drug Market, Biologic Therapy, HIV
Expert is an expert in EMEA drug regulation at it applies to marketed drugs. Drug regulation, he has knowledge in the steps that need to be met during pre-clinical and clinical drug development of drug candidates. He has expertise on the EMEA, ... See full profile | | Valencia, Spain | | | |  | | Expert in Drug Discovery & Development Technology and Intellectual Property (Patents, Trade Marks, etc.)
He has had the Drug Discovery Department, as part of his role as Director R & D, at Wockhardt Limited, discover several new NCEs during the tenure of this position, which NCEs are more extensively described in a later section of these summaries under the ... See full profile | | India | | | |  | | Expert in Pharmaceuticals, Clinical Pharmacology, Toxicology, Drug Development, Regulatory Affairs, Patents
Expert worked in pharmacological research concerning opiate analgesics. The objective of the research was to find an anti-diarrheal drug with minimum analgesic actions. In particular, he led the research team that discovered and developed nufenoxole, ... See full profile | | Illinois (IL), USA | | | |  | | Expert in Pharmaceutical Development, Analytical Methods, Method Validation and GMP/Part 11 Compliance
Expert has been involved with cGMPs since their re-release in March 1979. For 7 years during his tenure at Roche he was Compliance and Training Officer for the Technical Development and Kilo Lab Departments, and developed schemes by which the Pilot Plant ... See full profile | | New Jersey (NJ), USA | | | |  | | Expert in Hatch-Waxman patent litigation, CMC Pharma Dev Issues, Preformulation/Formulation, Regulat-Reports
As the development of a pharmaceutical reaches Phase 3, prior to submission of an NDA, method validation is required. Validation is a demonstration of optimization. By demonstrating the capacity of a method within the bounds of validation, optimal ... See full profile | | Florida (FL), USA | | | |  | | Expert in Pharmaceutical Development & Validation
Expert has over 20 years of broad-based experience with pharmaceutical product development. His work in this area has ranged from early phase 1 drug characterization to phase 4 market product launch and validation. See full profile | | Pennsylvania (PA), USA | | | |  | | Expert in Medicinal Chemistry, Synthetic Organic Chemistry, Drug Discovery, Pharmacokinetics
Expert has strong knowledge in asymmetric multi-step organic synthesis, scaffold design and library development with ability to solve challenging chemistry problems and have authored peer-reviewed articles and patents. Expert is a synthetic and ... See full profile | | Wisconsin (WI), USA | | | |  | | Expert in Parenteral/Sterile Product Formulation Development; Protein Peptide Formulation; Drug Delivery
Former Director, Formulation Research, Hoffmann-La Roche Inc.- primarily parenteral formulation and drug delivery systems – Extensive experience in the areas of formulation, drug delivery and clinical manufacturing - Member of Global Formulation ... See full profile | | New Jersey (NJ), USA | | | |  | | Expert in CRO in Medicinal Chemistry, Pharmaceutical Chemistry, API, CRAMS, Speciality Chemicals, Training
Expert received his PhD in synthetic organic chemistry from the University of Hyderabad. He has 2 years of post-doctoral experience in synthetic and physical organic chemistry from University of Houston. He also worked on chiral polymers and energetic ... See full profile | | India | | | |  | | Expert in Pharmaceutical Licensing, Life Science Licensing, Commercialization
Expert has worked with a number of pharmaceutical and life science companies at senior level as either employee, consultant or interim manager, supporting initial public offerings and other fundraising activities and cross-border M&A. See full profile | | Middlesex, United Kingdom | | | |  | | Expert in Drug Delivery, Formulation Development of NCE's, Preformulation, Stability, Clinical Manufacturing
She has been involved in contract manufacturing of pharmaceuticals for the drugs and devices. Contract manufacturing for drugs have included identification, evaluation, screening and selection of CRO's and CMO's in the area of sterile solution and oral ... See full profile | | California (CA), USA | | | |  | | Expert in Pharmaceutical Quality Assurance
He possess thorough knowledge of GMP / GLP regulations like US FDA, WHO GMP, ICH, MHRA, ANVISA, requirements of cGMP documents (SOP's/ Change controls/ Deviations) as per various regulatory agencies. He had actively participated in various international ... See full profile | | India | | | |  | | Expert in Pharmaceutical Drug Development, Strategic Executive Management, Biopharma Mergers and Acquisitions
Expert has over 20 years of experience. He is extensively active and has significant experience and expertise in Europe and the US in the areas of drug development and financing throughout Europe and the US. He was responsible for the overall ... See full profile | | Netherlands | | | |  | | Expert in Health and Personal Product Development
Expert brings 40 years of experience directing the development and evaluation of new and improved pharmaceutical and personal care products to assist you in managing the technical aspects of your business. In addition to developing several ... See full profile | | New Jersey (NJ), USA | | | |  | | Expert in Fluorescence Spectroscopy, Analysis of Metal Ions by Chelation with Organic Ligands, etc.
Fluorescence spectroscopy. Expert has worked in the area of fluorescence spectroscopy for almost thirty years. He has published extensively on the influences of pH and solvent composition upon fluorescence spectra and has used these ... See full profile | | Florida (FL), USA | | |  |
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