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Marko Krutyholowa
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GMP & FDA Biologics Guidance | Thermo Fisher Scientific - USThermo Fisher Scientific LogoThermo Fisher Scientific LogoSearch buttonSearch buttonClosePlus IconMinus IconPlus IconMinus IconPlus IconMinus IconPlus IconMinus IconPlus IconMinus Icon
FDA Outlines its Approach to Artificial Intelligence Regulation - MedTech Intelligence
Essential Market Research Studies for New Product Development in the Medical Device Industry - Cetas Healthcare
Citrix Autoscale: Optimizing Resource Allocation for Better User Experiences- Citrix Blogs
First Resonance | Use Cases | Solutions
Comparing risk-adjusted inpatient fall rates internationally: validation of a risk-adjustment model using multicentre cross-sectional data from hospitals in Switzerland and Austria - PubMedTwitterFacebookLinkedInGitHubTwitterSM-FacebookSM-Youtube
Saas market validation: Case Studies: Successful SaaS Products and Their Validation Journeys - FasterCapital
New Product Development Manufacturing Timelines Explained
What is procurement in the context of the automotive industry? | 4 Answers from Research papers
Novel Drug Approvals at FDA | FDA
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Marko Krutyholowa
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Marko Krutyholowa

Marko Krutyholowa

Principal at Concept to Commercialization at Concept to Commercialization

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Marko Krutyholowa

Marko Krutyholowa

Principal at Concept to Commercialization at Concept to Commercialization

Joined 09/19/2017

Level: LEVEL 01 (12 mo pts: 0 pts)

Rating: 4.9565/5 stars (23 ratings)

Lifetime points: 386 pts

My career focused on the development of innovative products and processes and has spanned several industries. Successes include developing and leading high-performing engineering teams, architecting business-critical cost saving and operational strategies, designing and implementing new and novel multi-million dollar manufacturing processes, and partnering internally and externally to manage the delivery of new product launches.
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