Metis Consulting Services
Pharmacovigilance Services, QA, Anaylsis, Process Development, Pre-Inspection Audit Readiness.

Metis Consulting Services

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Focused on today's deliverables for the future safety of patients and products.

Metis Consulting Services is a boutique consultancy serving Global Biotech and Pharmaceutical Industries. Services we offer include: Drug Safety and Pharmacovigilance, Gap Analysis, GXP Audits, Pre-Audit Inspection Readiness, REMS, SOP Implementation, Corporate Training, Quality Assurance, Medical Writing, Compliance, Scalable Implementation Planning, and Standardization of Services that create high impact experiences. All of our services are scalable for long term success, focused on today's deliverables for the future safety of patients and products.

Hustle. Deliver. Hustle. It's our motto.

Get in touch with us to set up a consultation, or use the Inquiry Form at the bottom of this page to share with us what you are up to and determine if our services are right for you.



☎ Call today (time zone: pdt)

(760) 443-2659


Vista, CA

“We must have perseverance and above all confidence in ourselves. We must believe that we are gifted for something and that this thing must be attained.”

MARIE CURIE, first woman to win the Nobel Prize in Chemistry

Consulting Services


Ideal of any size company with a drug in development, first in human trials, Phase I trials, Phase II trials or acquired compounds with no infrastructure system established. We will help you to assess the best team to present to the Inspectors, and identify of potential gaps. Learn more.


It is not just 21 CFR Part 11 anymore - compliance is interconnected across functions, and taking a landscape approach to your requirements may mean navigating unfamiliar territory for those of us more accustomed to working in a solo environment. Learn more.

Corporate training & ADVISING

Broaden the skills and improve understanding with training for your employees. Learn more.

As needed remote advising in a Q&A format. Learn more.


From a check up on existing structures to pre-inspection, inspection response for laboratory, pre-clinical, manufacturing, clinical, pharmacovigilance, and to post-marketing sectors, a gap analysis helps you target what you’re missing. Learn more.


Documentation covers a broad spectrum of targeted areas. Learn more.


May include areas from regulatory, alignment, redundancy, scalability, and much more. Learn more.



Let's Talk It Out

We'd love to hear from you!

You may email us directly at or fill out the Inquiry Form below.

If you would like us to call you back, please include optimal times to speak with you.

To speak to us over the phone, reach us at (760) 443-2659

Inquiry Form:

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Last updated: 29 March 2019