About Us
Our focus is compliance & business consulting to the personalized medicine industry (503A & 503B, cell & gene, high value GMP drug manufacturers).
Our focus is compliance & business consulting to the personalized medicine industry (503A & 503B, cell & gene, high value GMP drug manufacturers).
Our Clients Include
COMPOUNDERS - Hospitals, home infusion facilities, 503A compounding pharmacies, 503B outsourcing facilities
GMP BIO/PHARMA - Pharmaceutical & biologics manufacturers, contract drug manufacturers, cell & gene therapy labs
CLINICAL - Physician clinics & clinical trial research teams
OTHER - Cosmetic, OTC, and dietary supplement companies
ATTORNEYS - Law firms serving the healthcare and pharmaceutical industries
INVESTORS - Investment firms handling mergers and acquisitions
Who We Are
Our team is comprised of industry experts from multi-disciplinary backgrounds ranging from GMP pharmaceutical manufacturing to 503A & 503B compounding to cell & gene therapy. Each associate has several years of experience and is highly knowledgeable within a particular specialty.
For every project, we follow a simple onboarding process:
Discover
Your project requirements, timeline, & budget.
Select
The most qualified and prepared associate(s).
Deliver
Solutions that often exceed your expectations.
Once you become a client, we initiate a 5-step project sequence:
A kickoff meeting is an opportunity to introduce you to our project team, review the project brief, discuss milestone expectations, and how to make the project a success. This meeting happens before the project scope of work is initiated.
At this phase of the project, we will ask you to submit key documents, diagrams, and/or videos related to the project. This could be for example, an organizational chart, facility diagram and/or video footage, SOPs, product list, production records and/or video footage, training records, environmental monitoring data, regulatory/accrediting body application/inspection report, etc. Submitting this information is a rate-limiting step to moving the project forward. To make the process easier, you will be granted access to our private HIPAA-compliant portal, where you can securely submit the information and files requested.
Once the files have been shared, our project team reviews the information submitted, conducts project-specific research if applicable (e.g., market research, on-site gap analysis audit, formulation development, etc.), and makes an assessment as to the changes or additions that need to be developed and delivered to your company to meet the project goals.
If any major revisions, additions, or remediations are necessary to make the project a success, our team will alert your company at the time of finding.
The last step of the process is to develop and submit the deliverables (e.g., customized SOPs or protocols, CAPA plan and implementation, gap analysis report, etc.) according to the projected project timeline. Documents created will be submitted through the client portal. Other deliverables will be performed per project needs (e.g., staff augmentation, personnel training, expert witness testimony, etc.).