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Tablet Manufacturing Experts| The following experts are available as tablet manufacturing consultants and tablet manufacturing expert witnesses. Intota experts are peer-recommended authorities who have been carefully selected and rigorously screened. | |
| | Definition: Tablet Manufacturing -
The manufacturing of tablets. |
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| 1 to 25
(of 37) | | | Tablet Manufacturing Experts |
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Expert Quote | | |  | | Expert in Powders and Tablet Manufacturing
Expert has developed tableting systems and products in the areas of pharmaceuticals, diagnostics, high-protein snack products, chlorine tablets, chlorine removal tablets, over the counter antacids, and vitamins. See full profile | | Michigan (MI), 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 Legacy Application Support: Manage, Measure, Improve Using ITIL V3 Service Management Life Cycle
Expert spent 10 years as Director of MIS for the Revlon Health Care, Pharmaceutical Division and managed all IT activities for 5 companies within the division. Major accomplishments were designing and implementing complex pharmaceutical order ... See full profile | | Pennsylvania (PA), USA | | | |  | | Expert in Pharmaceutical Development; X-ray Computed Tomography; Tabletting; Particle Technology
Expert has extensive experience in numerical modelling particulate material manufacturing and characerisation, modelling and characeristion of the behaviour of particulate materials during the manufacturing processes for pharmaceutical and other ... See full profile | | United Kingdom | | | |  | | 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 Validation
Expert has been an independent Validation Consultant for around 10 years; he is responsable for the management of validation projects. He supervises resources acting as a project manager and is also responsible for the development and execution of ... See full profile | | Puerto Rico | | | |  | | Expert in Orphan Drugs: FDA/EU/Canada; FDA Approval; Drug Development: CMC, QA, QC, Manufacturing
12 product approvals from FDA including 6 new chemical entities, a 510k device, and three major pharmaceutical efficacy indication supplemental approvals. All received 5-10 years of regulatory exclusivity (Hatch-Waxman, Orphan Drug). See full profile | | Minnesota (MN), USA | | | |  | | 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 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 Green Energy Controls, Automotive Manufacturing, Pharmaceutical Process Controls
Expert has designed patented systems which increase manufacturing productivity, flexibility, and quality while drastically reducing inventory in discrete and continuous manufacturing industries such as automotive, machine tool, pharmaceutical ... See full profile | | Indiana (IN), USA | | | |  | | Expert in Regulatory Affairs, Technology Management, Pharmaceutical Industry, Turnaround Management
Expert has experience in applying 21 CFR Part 11 to the manufacturing of pharmaceuticals and preparing and facing FDA inspections. He has more than 20 years of experience in various facets of API industry ranging from research to manufacturing, ... See full profile | | Maharashtra, India | | | |  | | Expert in Pharmaceutical Facilities, Pharmaceutical Manufacturing Processes, Facility FDA Compliance
In addition to having primary responsibility for numerous pharmaceutical construction projects over the last 15 years, Expert has also held several positions with pharmaceutical and medical device companies where he was responsible for the daily ... See full profile | | Colorado (CO), USA | | | |  | | Expert in Pharmaceutical Development, CMC, Project Management, Intellectual Property
Expert has developed modified release products throughout his career. Most recently he led the development of proprietary oral modified release systems at Phoqus Pharmaceuticals. These included zero-order, increasing-rate, pulsatile, delayed-release, ... See full profile | | Kent, United Kingdom | | | |  | | Expert in Pharmaceutical, Cosmetics and Nutritional Supplements Product Development and Production
Expert has applied his pharmaceutical and cosmetic technology backgrounds to the development of fast acing and very effective after shaves especially aftershaves for problem skin. He has formulated soothing and conditioning aftershaves with natural and as ... See full profile | | Massachusetts (MA), USA | | | |  | | Expert in FDA Compliance, Project Management, New Product Development, Validation, Cultural Transformation
Expert has audited many cGMP operations. A good audit starts with a good plan. Before starting an on-site audit, he reviews past audits. He notes indications of possible problem areas and items, if any, that were identified for corrective action in a ... See full profile | | Michigan (MI), 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 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 Analytical Chemistry, Analytical Technology Development and Application
Expert is a Ph.D. Pharmaceutical Analytical Chemist with extensive experience in separations (LC, GC, Prep GC), dissolution, automation (robotics, computers) and general analytical technologies. He has familiarity with NDA programs and marketed product ... See full profile | | Florida (FL), USA | | | |  | | Expert in Practical Application of GLP, GCP, and cGMP to Pharmaceutical, Device, and Biotechnology Firms
As Vice President at a pharmaceutical company, Expert formulated eight pharmaceuticals for use in their patented buccal delivery platform technology. Five formulations were acceptable to FDA and were allowed to proceed into ... See full profile | | New Jersey (NJ), USA | | | |  | | Expert in Biotechnology Product Reviews, Biologics, Drugs & Medical Devices, FDA Litigation, Vaccines, etc.
Over 18 years experience with legal, scientific, business and regulatory issues affecting the research, development and commercialization of biomedical and information security products. Recognized expertise in strategy development, audit and due ... See full profile | | Virginia (VA), USA | | | |  | | Expert in Aseptic Process Design, Airflow Visualization, HACCP, PAI Preparation, Cleaning Validation
Expert has performed validation of aseptic processes including technologies such as blow-fill-seal, high-speed automated liquid and powder filling lines, lyophilization, barrier and isolation technology, and bulk pharmaceutical and biological ... See full profile | | New Jersey (NJ), USA | | | |  | | Expert in Industrial Statistical and Quality Control Applications
Expert is knowledgeable and experienced in the industrial application of attribute sampling standards (MIL-STD-105 / ANSI Z1.4) and variables sampling standards (MIL-STD-414 / ANSI Z1.9) to acceptance sampling inspection, which ... See full profile | | New Jersey (NJ), USA | | | |  | | 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 Mixing, Pilot Plants, Scaleup, Atomization, Agglomeration, Evaporation, Heat Exchangers
Expert has extensive knowledge of mixing operations needed in the chemical, petrochemical, and biochemical industries. His knowledge includes the proper selection of effective mixing geometries and the power requirements needed by a mixing ... See full profile | | North Carolina (NC), USA | | | |  | | 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 | | |  | | >> Next 25 Experts
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