Introducing a unique opportunity to enhance your skills through consultation services with experts in the field of pharmaceutical compounding.
Introducing a unique opportunity to enhance your skills through consultation services with experts in the field of pharmaceutical compounding.

Specialized Consultation Services

Consult with our Team of Experts

Introducing a new line of on-site and off-site services that will allow you to fulfill all of your pharmacy`s operational needs, by connecting with one of our experts in the field of pharmaceutical compounding.

Choose the Regulatory Compliance Package that Meets your Pharmacy Needs:

Lab Design Support
  • Up to 7 hours off-site lab design support.
  • Review of current/proposed lab layouts and/or blueprints.
  • Provide recommendations and strategies for new compliant lab.
  • Provide preliminary design drafts for architects/engineers.
USP Compliance Assessment
  • 1-day on-site assessment; evaluation pharmacy’s facility and operations towards applicable USP standards of practice.
  • Post-assessment; submission a findings and remediation report by consultant.
503B Mock FDA Inspection
  • 2-day on-site assessment; evaluation of facility and operations towards compliance expectations of a registered 503B outsourcing facility, of the cGMP requirements per 21 CFR part 211 and of the FDA.
  • Post-assessment; submission a findings and remediation report by consultant.
PCAB/ACHC Mock Accreditation Survey
  • 1-day on-site assessment; evaluation pharmacy’s facility and operations towards PCAB/ACHC standards of practice.
  • Post-assessment; submission a findings and remediation report by consultant.
NABP VPP Mock Inspection
  • 1-day on-site assessment; evaluation pharmacy’s facility and operations towards NABP VPP regulation standards.
  • Post-assessment; submission a findings and remediation report by consultant.
DEA Mock Audit
  • 1-day on-site assessment; evaluation pharmacy’s facility and operations towards applicable DEA and Controlled Substances laws and regulations.
  • Post-assessment; submission a findings and remediation report by consultant.

Other Specialized Services Include:

  • Facility Lab Design & Operation Support
  • USP <795>, USP <797> and/or USP <800> Compliance Analysis
  • FDA Form 483 Remediation Support
  • State Board of Pharmacy Compliance Monitoring
  • Current Regulatory Landscape and Proposed Changes
  • Customization of Policies and Procedures (SOPs)
  • Quality Assurance and Continuous Quality Improvement
  • Long-term Care Operational Efficiency & Clinical Improvement
  • Strategic Organizational Processes
  • Patient Care Compliance Programs
  • Nuclear Pharmacy & Nuclear Medicine
  • Acquisition and Strategic Planning
  • Niche Market Specific Questions
  • Clinical Inquiries

Take advantage of this unique opportunity and have a MEDISCA Network Account Executive contact you today!

Schedule your one-on-one consultation with top experts in the industry!




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