BioTeknica is a consulting firm specializing in regulatory compliance, FDA inspection readiness, quality engineering, and validation projects for the Medical Device, Biologics, and Pharmaceutical industries.

We have a solid track record of providing resolution for FDA compliance and validation issues.

S 3 – Simple, Systematic and Sustainable Solutions for Today’s Evolving Regulatory Environment


Because the probability of success increases the earlier and more thoroughly you prepare – and our proven methodologies fully prepare your organization for any regulatory challenge. We pride ourselves on prompt response times and our diverse and unique technical skillsets to fully service your organization.


Our Corporate Quality Policy

BioTeknica will continuously strive to:

Our Core Values

  • A strong passion and pride for the quality of service and the importance of what we do  
  • The collective knowledge and expertise of our staff and associates 
  • To inspire trust with our clients and associates  
  • To remain a recognized leader in our industry  
  • To take responsibility individually and collectively being collaborative with our clients and one another
  • A “Family and friends”- driven work culture 
  • Community service involvement

Our Vision

We aim to improve healthcare by partnering with medical device and pharmaceutical manufacturers to enhance their product quality, safety, and effectiveness.

Our Mission

We will accomplish our vision by establishing and developing the best team in the industry who embraces BioTeknica’s core values and provide them with a workplace environment that stimulates professional growth and satisfaction.