Our Guiding Principles
Collaborative
We collaborate and communicate effectively with your organization and those you work with.
Adaptable
Our team understands and is ready to meet the variable and rushed demands of the development lifecycle.
Driven
At Cadoret, we know how to wear multiple hats and assist our Clients with prioritization of work.
Organized
Our niche is to give companies a hand in setting a foundation for success through procedures, processes and scalable, phase-appropriate systems.
Reliable
We are willing to go the extra mile for your success.
Experts
We have proven experience in helping companies like yours lay the foundation for Quality and Compliance from the get-go.
Timely
At Cadoret, we know deliverables and timelines impact the bottom line, and prioritize accordingly.
Cadoret Global was established on the premise that consultants are partners invested in the success of their Clients.
We specialize in supporting start-up, virtual, early-stage, and small-size pharmaceutical companies in taking their investigational drug through development and clinical trials.
Our aim is to provide high-caliber and phase-appropriate Quality Assurance consulting services tailored to our clients’ budget and timelines.
We are here to support our Clients with:
the progressively complex and time-sensitive requirements of getting investigational drugs through development and clinical trials
the pressing need for a phase-appropriate Quality Management System that runs in parallel with the development lifecycle and is tailored to support both on-site and virtual teams
the risk-based and relationship-driven qualification and oversight of outsourced manufacturing, testing, storage and distribution of clinical trial materials
Let’s discuss your needs!
Founder
Principal Consultant
Enith Morillo
Dependable and versatile Senior Quality Assurance professional and CGMP Auditor with 15+ years of experience in the FDA and DEA regulated pharmaceutical field.
Proven experience in supporting emerging, early stage and virtual pharmaceuticals throughout the drug development lifecycle to clinical trials. Adept collaborator with CMC and CMO teams in ensuring phase-appropriate, quality operations that span from starting materials to the drug product and successful regulatory filings. Experience in taking drugs from development through validation, PAI, and commercialization.
Expertise encompasses CGMP auditing, domestic and internationally, of API and DP manufacturers, contract laboratories, packagers, and distributors, among others.
Predominant experience with small molecule, oral solid dosage forms, but have worked with gene therapy and biopharmaceutical products.
She holds a Masters and Bachelors of Science in Electrical and Biomedical Engineering from Worcester Polytechnic Institute.
Enith enjoys traveling, writing, and mentoring others.