Our Experts
CriticalPoint empowers pharmacists, pharmacy technicians, inspectors, and healthcare professionals with essential skills to improve performance and ensure safety in compounding environments. With an expansive library of virtual trainings, support resources, and industry-leading learning solutions, CriticalPoint is the trusted resource for those seeking compliance and excellence. Our comprehensive courses cover everything from compounding best practices to inspector training, offering multimedia solutions tailored to your needs. Plus, with our complimentary CE/CME & Training Organizer, managing license requirements and course completions has never been easier.
Strengthen your compounding operations with CriticalPoint—because patient safety and quality are non-negotiable.
Tasha Jackson - BS, PharmD, PCSCP
Editor - CriticalPoint
Dr. Latousha P. Jackson is a Doctor of Pharmacy with over 18 years of experience in pharmacy practice, bringing a wealth of knowledge and expertise to sterile compounding. Her qualifications are demonstrably suited to delivering informative and engaging lectures for sterile compounding pharmacies.
Prior to joining the CriticalPoint team, Dr. Jackson served as the Compounding and Hazardous Medication Compliance Program Manager with the U.S. Department of Veterans Affairs in Durham, NC. Dr. Jackson also obtained Board Certification in Compounded Sterile Preparations (BCSCP).
Deep Understanding of Sterile Compounding Regulations:
- Board-Certified Sterile Compounding Pharmacist with a proven track record of ensuring compliance with USP chapters (795, 797, and 800).
- Extensive experience in developing and implementing programs to maintain sterile compounding practices that meet national standards and best practices.
- Proven ability to translate complex regulations into clear and actionable guidance for pharmacy personnel.
Leadership in Sterile Compounding Implementation:
- Previously served as Program Manager for Compounding and Hazardous Medication Compliance at the VA Health Care Systems.
- Led key projects such as the implementation of software systems (Simplifi 797 and Omnicell IVX) specifically designed to enhance sterile compounding compliance.
- Demonstrated leadership skills in overseeing the development and execution of a comprehensive quality assurance program for sterile compounding within a large healthcare system.
Commitment to Knowledge Sharing and Education:
- Currently serves as Managing Editor at TRC Healthcare, overseeing the creation of evidence-based reference documents on sterile compounding.
- Actively involved in professional organizations like the ASHP Section Advisory Group on Medication Safety, fostering collaboration and knowledge exchange on best practices in compounding.
- Experienced lecturer with a talent for translating complex topics into clear and engaging presentations.
Dr. Latousha P. Jackson's dedication to patient safety and her extensive experience in sterile compounding regulations make her an ideal resource for pharmacies seeking to enhance their compounding practices. Her ability to communicate complex information effectively ensures that attendees gain valuable knowledge and practical skills.
Adam J. West - RCP-SCF & NSF/ANSI
Environmental Monitoring and Training Specialist
Adam has nearly two decades of experience in the certification industry providing field certification services for 503A and 503B sterile compounding facilities and pharmaceutical and medical device manufacturers. In addition to certification, he has extensive knowledge in viable environmental monitoring, including sampling plan development and remediation and has provided consultation services for USP Chapter <797> facility design compliance. Adam held CETA's Registered Certification Professional – Sterile Compounding Facilities (RCP-SCF) certification and NSF-49 accreditation for numerous years until he no longer performed certification in the field.
In his current role, he is responsible for the development of live training curriculum and eLearning for sterile compounding pharmacy staff seeking to advance their skills, reinforce fundamental knowledge and implement best practices for USP compliance. He also provides consulting for environmental monitoring investigations and remediation, facility design of primary and secondary engineering controls for sterile compounding facilities, as well as pharmacy operation evaluations.
Lecturer/Other Activities:
2022
- CETA's CAG committee member and technical writer – Revision of CAG-005 Servicing Hazardous Drug Compounding Primary Engineering Controls
2021
- PDA Midwest Chapter – Webinar panelist “Cleanroom and Compounding Environmental Control”
- Pharmacy Purchasing & Products (PPMAG) - Technical writer/peer reviewer “Choosing the Right Cleanroom Construction Approach”
- Institute of Environmental Sciences and Technology (IEST) ESTECH 2021 Virtual Conference – Co-lecturer “Cleaning, Disinfecting, and Considerations for Facility Design in Sterile Compounding”
- Pharmacy Purchasing & Products (PPMAG) - Technical writer/peer reviewer “Understanding Cleanroom Certification Reports”
2020
- Pharmacy Purchasing & Products (PPMAG) - Technical writer/Author “Operational Compliances Drives Cleanroom Design”
2019
- CriticalPoint Center for Training and Research Faculty Member
2018
- Controlled Environment Testing Association CETA Keynote Speaker – Adopting or Adapting? Handling Customer Documentation as it Relates to Current Industry Standards
- Controlled Environment Testing Association CETA Series Presenter – Performing Fingertip Gloved Sampling
2014
- Controlled Environment Testing Association (CETA) Application Guide – 009 Working Group Member
- Controlled Environment Testing Association CETA Series Presenter – Performing Fingertip Gloved Sampling
Organizations and Associations
- Parenteral Drug Association (PDA)
- Controlled Environment Testing Association (CETA)
- National Home Infusion Association (NHIA)
- American Society of Health-System Pharmacists (ASHP)
- Institute of Environmental Sciences and Technology (IEST)