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An Overview for Panelists: Sunscreen Effectiveness Testing New sunscreen products are always in development, and companies look for people like you to help with Sunscreen Effectiveness Testing. Sunscreens may be tested on any attribute from sand- or water-resistance to the extent of broad-spectrum protection. Most often, sunscreens are tested on
How Can FDA Compliance Consultants Benefit Your Next Product Launch? Before an OTC Drug or even a cosmetic/personal care product can be brought to market in the US, it must first undergo conceptualization, development and a rigorous testing process to ensure that it meets FDA requirements for safety (cosmetic/personal care
Virtually all Over-the-Counter (OTC) and Prescription (Rx) drug products distributed within the USA are required to display an expiration date on their labeling. Expiration dates must be supported by stability testing, which has been conducted in accordance with current FDA and ICH Guidelines and cGMP requirements. Each strength of a
A 48 hour patch test performed in healthy volunteers to determine the presensitization (pre-existing allergy) of Neo-Synalar (neomycin sulfate 0.5%(0.35% neomycin base), fluocinolone acetonide 0.025%) Cream . Subjects also receive a positive control (Sodium Lauryl Sulfate) and a negative control (Saline). The primary objective of this study was to determine
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An Overview for Panelists: Sunscreen Effectiveness Testing New sunscreen products are always in development, and companies look for people like you to help with Sunscreen
How Can FDA Compliance Consultants Benefit Your Next Product Launch? Before an OTC Drug or even a cosmetic/personal care product can be brought to market
Virtually all Over-the-Counter (OTC) and Prescription (Rx) drug products distributed within the USA are required to display an expiration date on their labeling. Expiration dates
A 48 hour patch test performed in healthy volunteers to determine the presensitization (pre-existing allergy) of Neo-Synalar (neomycin sulfate 0.5%(0.35% neomycin base), fluocinolone acetonide 0.025%)
NYSCC
New York, New York
5/1 – 5/2
Booth 519
Excipient World
Orlando, Florida
5/13 – 5/14
Booth 101
Corporate Headquarters and Labs
70 New Dutch Ln
Fairfield, NJ 07004
973-576-5957
Second Clinical Lab Location
304 Wootton St.
Boonton, NJ 07005
FDA
Registration# 1000151293
DEA
Registration# RC0199744 (Analytical Lab)
Schedule I-V license
Remember, Schedules I-II require DEA Form 222
Registration# RC0171568 (Researcher)
US EPA/NJ DEP
Registration# NJD982726648