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      Details

      Your Partners in Compliance

      General Info

      Over thirty years experience in the pharmaceutical / medical device industry. Track record of instituting and maintaining high levels of Quality Assurance, and leadership in the pharmaceutical, medical devices and biological industries. Experts in compliance, auditing, investigations, product complaint, validation, SOP development and assessment, PDMA, cGMP, CFR, document control (First Docs, Documentum, etc.), State and Government regulations, inspections, SOP Development, Quality Control, FDA Regulations, Regulatory Affairs, change control. Expertise in all industry related ISO regulations. Experience in European regulatory body regulations, Utilities/Facility and equipment validation.

      HoursCLOSED NOW
      Regular Hours:
      Mon - Fri
      Sat - SunClosed

      Contact Info

      Phone:

      Main - 888-429-4624

      Address:
      PO Box 370 Chesnee, SC 29323
      Email:

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      Category
      Computer Software & Services
      Services / Products
      FDA Compliance Computer System Validation Internal Audits Vendor Audits Supplier Audits CFR Chapter 21 Part 11 Audits CFR Chapter 21 Part 203 & 205 PDMA Audits CFR Chapter 21 Part 820 Audits
      Associations
      Associated with all the major pharmaceutical companies in the industry
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      Data provided by one or more of the following: Thryv, Data Axle, Yext.