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| Over 35 years experience of trial experience, Biomedical Science, Toxicology and Regulatory Compliance for Drugs, Biologics, Diagnostics and Pesticides. Well-versed in Drug and Medical Product Development, licensing, patents and acquisitions....
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| Forensic toxicologist with 22 years drug and alcohol testing experience
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| Expert in Industrial Engineering, Operations/Logistics Management, Automation Systems & Equipment, Material Handling Equipment, and MRP, WMS, DCS, MHS, and TMS Software Integration.
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| Industrial & Utility power generation and cogeneration expert. 30 years hands-on experience with plants from 100 kW to 1,000 MW. Extensive International experience arbitrations & litigations expert.
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| Experienced pharmaceutical scientist able to assist in litigation involving scientific evidence as well as patents and trademarks to include evaluation of science issues relevant to business mergers.
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| Scientist, Farmer, Programmer and Court Certified Expert Witness in Pennsylvania.
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| Marketing, sales, & market research. Specializing in biotechnology & life sciences: molecular biology research tools, molecular diagnostics, pharmaceuticals. Testimony & litigation support experience
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| Over 30 years experience in testing all phases of paints, sealants and waterproofing materials. Extensive knowledge of test methods and testing protocol.
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| A recognized expert in telecommunications, computer telephony and facsimile. 22 years of telecom product development, marketing, sales and service experience.
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| A Registered Dietitian with nine years of experience.
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| Senior Scientist, CSC. Previously VP of R&D at Aerotech Laboratories. Co-inventor of two patents, recipient of an NIH grant, and a co-author on more than 40 publications and 40 proceedings.
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| Specializes in the Forensic Analysis of all types of digital assets and media (Computer Forensics) for law firms and corporate clients.
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| Looking for a pharmaceutical data management expert?
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Find Pharmaceutical Data Management experts and consultants for Pharmaceutical Data Management litigation support at www.expertwitness.com. Available to be Pharmaceutical Data Management expert witnesses and provide Pharmaceutical Data Management forensic consulting in Pharmaceutical Data Management litigation, in addition prepare Pharmaceutical Data Management expert witness reports for use in deposition and/or in-court trial testimony.
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Categories To Find "Pharmaceutical Data Management" Experts:
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ADVERTISING |
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Firms in the advertising and public relations services industry prepare advertisements for other companies and organizations and design campaigns to promote the interests and image of their clients. This industry also includes media representativesÂfirms that sell advertising space for publications, radio, television, and the Internet; display advertisersÂbusinesses engaged in creating and designing public display ads for use in shopping malls, on billboards, or in similar media; and direct mail advertisers. A firm that purchases advertising time (or space) from media outlets, thereafter reselling it to advertising agencies or individual companies directly, is considered a media buying agency. Divisions of companies that produce and place their own advertising are not considered part of this industry.
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ANTITRUST |
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Antitrust or competition laws are laws which seek to promote economic and business competition by prohibiting anti-competitive behavior and unfair business practices. Government agencies known as competition regulators regulate antitrust laws, and may also be responsible for regulating related laws dealing with consumer protection.
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D.O.T. / REGULATORY COMPLIANCE |
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The United States Department of Transportation (DOT) is a Cabinet department of the United States government concerned with transport. It was established by an act of Congress on October 15, 1966 and began operation on April 1, 1967. It is administered by the United States Secretary of Transportation.
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DUE DILIGENCE |
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Due diligence (also known as due care) is the effort made by an ordinarily prudent or reasonable party to avoid harm to another party or himself. Failure to make this effort is considered negligence. Quite often a contract will specify that a party is required to provide due diligence.
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INTELLECTUAL PROPERTY - ANALYSIS |
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In law, intellectual property (IP) is a broad entitlement extending the concept of property beyond its materialist definitions to include information, ideas, and other intangible assets in their expressed form. Depending on jurisdiction, IP rights generally enable the holder to exercise exclusive rights over the the subject matter (or "work") of the IP using copyright, patent, trademark, industrial design right and similar legal protections. The term reinforces that such works are the product of the mind or intellect and that any rights may be protected at law in the same way as any other form of property.
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INTELLECTUAL PROPERTY - LICENSING |
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In law, intellectual property (IP) is a broad entitlement extending the concept of property beyond its materialist definitions to include information, ideas, and other intangible assets in their expressed form. Depending on jurisdiction, IP rights generally enable the holder to exercise exclusive rights over the the subject matter (or "work") of the IP using copyright, patent, trademark, industrial design right and similar legal protections. The term reinforces that such works are the product of the mind or intellect and that any rights may be protected at law in the same way as any other form of property.
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ISO 9000 |
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ISO 9000 is an ISO standard for Quality Management Systems.
ISO 9000 was developed from the British Standards Institution's BS 5750. The ISO 9000 standard is maintained by ISO (the International Organization for Standardization) and administered by accreditation and certification bodies. It is widely used in manufacturing, although high costs and difficulties with implementation have led to many companies using alternatives such as IC9700, or IC9200, both of which are issued by the International Charter, or their own specific in-house 'standard'.
Some countries re-label ISO 9000 as a national standard. (e.g. IR 9000 in Iran).
It should be emphasised that ISO 9000 does not guarantee the quality of the end products - rather, it certifies that the correct manufacturing process is being carried out.
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MERGERS / ACQUISITIONS |
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The phrase mergers and acquisitions or M&A refers to the aspect of corporate finance strategy and management dealing with the merging and acquiring of different companies as well as other assets. Usually mergers occur in a friendly setting where executives from the respective companies participate in a due diligence process to ensure a successful combination of all parts.
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QUALITY ASSURANCE |
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In engineering and manufacturing, quality control and quality engineering are involved in developing systems to ensure products or services are designed and produced to meet or exceed customer requirements and expectations. These systems are often developed in conjunction with other business and engineering disciplines using a cross-functional approach.
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REGULATORY COMPLIANCE |
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Regulatory compliance refers to systems or departments at corporations and public agencies to ensure that personnel are aware of and take steps to comply with relevant laws and regulations.
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Pharmaceutical Data Management Experts Witnesses - Pharmaceutical Data Management Forensic Consultants.
Find Pharmaceutical Data Management experts and consultants for Pharmaceutical Data Management litigation support. Available to be Pharmaceutical Data Management expert witnesses and provide Pharmaceutical Data Management forensic consulting in Pharmaceutical Data Management litigation, in addition prepare Pharmaceutical Data Management expert witness reports for use in deposition and/or in-court trial testimony.
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Pharmaceutical Data Management
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