76 Consultants: Device

	DE - Newark	QPS is a GLP/GCP-compliant global full-service CRO providing discovery, preclinical services, bioanalysis, clinical trials, and clinical drug development. We deliver custom-built research services in Pharmacology, Toxicology, DMPK, Bioanalysis, Cell Therapy Products, Clinical Trials, and Clinical Development.
ABX-CRO	Germany - Dresden	Contract Pharmaceutical Research
ACA Pharma Concept	Germany - Leipzig	Pharma Consulting
Accumedix	IL - Libertyville	Medical Device Commercialization
Advena	UK - Bromsgrove	Medical Device Regulatory Consulting
Advena	UK - Warwick	Medical Device Regulatory Consulting
Alira Health	MA - Framingham	Consulting, Clinical Research
Archimedic	PA - West Chester	Medical Device Consulting
Asia Regulatory and Quality Consultancy	Singapore - Singapore	Medical Device Registration Services
Atessia	France - Paris	Pharma Consultancy
Baugher Consulting	PA - Philadelphia	Pharmaceutical, Medical Device QA Consulting
Bioacuity Consulting	ON - Oakville	Plasma protein therapeutics, biologics, drugs, medical devices development, manufacturing, operations, quality, compliance & regulatory consulting
BioBoston Consulting	MA - Boston	Quality & Regulatory Consulting
Biologics Consulting	VA - Alexandria	Full-service regulatory and product development consulting firm for biologics, pharma and medical devices
Biotech Research Group	FL - Tampa	Regulatory and product development consulting firm
Canyon Labs	UT - Bluffdale	Pharma & Device Consulting
Caraballo Consulting	FL - Doral	Pharmaceutical & Biotech Consulting
CatalystBio	IL - Chicago	Advisory services and fractional leadership
Celegence	IL - Downers Grove	Global Regulatory Consulting
Cell Bridge Strategies	TX - Boerne	Life Science, Regenerative Medicine & Cell Therapy Business Consulting
Chrysoli Consulting	FL - Orlando	Market Access Consulting
Clinqure	- Virtual	Clinical, Quality & Regulatory Services
CMD Medtech	OH - Columbus	Medical Device Development
CMIC	Japan - Tokyo	Pharmaceutical Contract Work
CMIC	NJ - Cranbury	Pharmaceutical Contract Work
Concise Engineering	FL - Clearwater	Medical Device Engineering Consulting
CTNT	Israel - Timorim	Clinical Development Services
EdgeOne Medical	IL - Wheeling	Combination Product Consulting
Emergo by UL	TX - Austin	Medical device consulting
Explicat Pharma	Germany - Hohenbrunn	Contract Research & Consulting
Farmigea	Italy - Pisa	Ophthalmology products (drugs, medical devices, and food supplements), contract development/manufacturing
Foothill Scientific Associates	CA - Lake Forest	Corporate / product development, technical management, and US funding for drug/device development
FPrin	CA - San Jose	Medical Device Consulting
G & H ITL	NY - Rochester	CDMO providing end-to-end design and manufacturing services for medical devices, in-vitro diagnostics, and laboratory instruments
G & H ITL	UK - Ilminster	CDMO providing end-to-end design and manufacturing services for medical devices, in-vitro diagnostics, and laboratory instruments
Gener8	CA - Carlsbad	Medical Devices Prototyping, Engineering & Design; Biotech Consumables
Gener8	CA - San Jose	Medical Devices Prototyping, Engineering & Design; Biotech Consumables
Gener8	MA - Wilmington	Medical Devices Prototyping, Engineering & Design; Biotech Consumables
GLOBAL Exponential Technologies	WA - Tukwila	AI/ML regulatory compliance software
GXP Consulting	Switzerland - Lausanne	Pharma, Device, Biotech Consulting
HaA Product Development	MA - Wakefield	Medical Device Strategy
HiTech Health	Ireland - Ballynahown	Biopharm CDMO
HiTech Health	Ireland - Dublin	Biopharm CDMO
HiTech Health	Ireland - Spidéal	Biopharm CDMO
Inizio Ignite	NY - New York	Commercialization Consulting
Innovative Device Technologies	CA - Fremont	Product Development
Intune	CA - Pasadena	IVD or medical device product development, analytical & clinical validation, regulatory approval
KB-DG	MA - Worcester	Pharma, Biotech, Device Consulting
Kymanox	NC - Morrisville	Life Science Consulting
Lumbar Healthtech	India - Chennai	Medical Device Registration & Approval in India
Medicept	MA - Ashland	Medical Device Compliance Consulting
Medsurgpi	NC - Franklinton	Medical Affairs Consulting
MinnHealth	MN - Minneapolis	MedTech R&D
Network Partners Group	IN - Warsaw	Medical Device & Pharmaceutical Consulting
NIU Consulting	Italy - Torino	Medical Device Consulting
Noble Life Sciences	MD - Woodbine	Preclinical CRO, Drug, Vaccine & Devices, GLP and non-GLP, Small & Large Animals, FDA, OLAW, AAALAC
Nucro-Technics	ON - Toronto	Contract Testing
OCLAD Engineering	TX - Houston	Life Science Engineering and Business Intelligence, Outsourcing and Contract Services
OMO Consultants	UK - ZZ	Biopharmaceutical & Medical Device Consulting
Ontogen Medtech	IL - Lisle	Medical device development services
Ossacur	Germany - Oberstenfeld	Medical Device Consulting - Development & Marketing
PaxMed	CA - Carlsbad	Medical Device Regulatory Consulting
Pharmaceutical Development Group	FL - Tampa	Regulatory Consulting
PQE Group	Italy - Reggello	Medical Device Consulting
ProPharma Group	CA - San Diego	Consulting
ProPharma Group	DC - Washington	Consulting
ProPharma Group	IL - Deerfield	Consulting
ProPharma Group	MT - Bozeman	Consulting
ProPharma Group	NC - Raleigh	Consulting
ProPharma Group	OH - Westlake	Consulting
ProPharma Group	ON - Windsor	Consulting
ProPharma Group	PA - Fort Washington	Consulting
Qnova LifeSciences	MD - Columbia	Consulting, Clinical Trial Enrollment
	DE - Newark	QPS is a GLP/GCP-compliant global full-service CRO providing discovery, preclinical services, bioanalysis, clinical trials, and clinical drug development. We deliver custom-built research services in Pharmacology, Toxicology, DMPK, Bioanalysis, Cell Therapy Products, Clinical Trials, and Clinical Development.
	FL - Miami	QPS is a GLP/GCP-compliant global full-service CRO providing discovery, preclinical services, bioanalysis, clinical trials, and clinical drug development. QPS Miami is a stand-alone full service Clinical Trials Unit, with a safety lab and a PBMC lab.
	India - Hyderabad	QPS is a GLP/GCP-compliant global full-service CRO providing discovery, preclinical services, bioanalysis, clinical trials, and clinical drug development. QPS India is a stand-alone full service Clinical Trials Unit, with a Bioanalysis lab for clinical trial sample analysis.
	MO - Springfield	QPS is a GLP/GCP-compliant global full-service CRO providing discovery, preclinical services, bioanalysis, clinical trials, and clinical drug development. QPS Missouri is a stand-alone full service Clinical Trials Unit, with a central safety lab, PBMC lab and leukopak (cell therapy) facility.
	Netherlands - Groningen	QPS is a GLP/GCP-compliant global full-service CRO providing discovery, preclinical services, bioanalysis, clinical trials, and clinical drug development. We deliver custom-built research services in Bioanalysis for small and large molecules and gene therapy.
	Taiwan - Taipei	QPS is a GLP/GCP-compliant global full-service CRO providing discovery, preclinical services, bioanalysis, clinical trials, and clinical drug development. QPS Taiwan (CTPS) is a full service Discovery, Preclinical, Toxicology and Pharmacology laboratory.
	Taiwan - Taipei	QPS is a GLP/GCP-compliant global full-service CRO providing discovery, preclinical services, bioanalysis, clinical trials, and clinical drug development. QPS Taiwan (Qualitix/NKSP) is a full service Clinical Trial Services division, with a Bioanalysis lab for clinical trial sample analysis.
Qserve Group	Netherlands - Arnhem	Quality, Regulatory, Clinical Consulting
RQM+	PA - Monroeville	Regulatory compliance consulting
Shields Pharma	ON - Markham	Psychedelic analytical testing and Contract testing lab
Smart Pharma Consulting	Netherlands - Hoofddorp	Pharma Consulting
Smart Pharma Consulting	PA - West Chester	Pharma Consulting
Square-1 Engineering	CA - Irvine	Medical device consulting - R&D, Quality, Compliance, RA, Manufacturing
Starodub	Netherlands - Nuland	Regulatory Consulting
Symogen	India - New Delhi	Pharmacovigilance, pharmacoepidemiology, medical writing, and regulatory affairs services
Symogen	UK - Marlow	Pharmacovigilance, pharmacoepidemiology, medical writing, and regulatory affairs services
Team Consulting	UK - Cambridge	Medical technology design and development consultancy
TentaConsult Pharma & Med	Germany - Münster	Pharma Device Consultancy
Texcell	MD - Frederick	Contract Research
The Windshire Group	MA - Cambridge	Development, manufacturing, technology transfers, due diligence, laboratory operations consulting
ThinkMedTek	IN - Indianapolis	Medical Device Design & Engineering
Uncommon Innovation	PA - Philadelphia	Medical Device Design & Regulatory Consulting
ValSource	PA - Downingtown	Life Sciences Strategy Consulting
Vectorb2b	Portugal - Lisbon	CDMO, CRO Services
Velentium Medical	TX - Richmond	Design and manufacturing of therapeutic and diagnostic active medical devices
Veranex	NC - Raleigh	Medtech Consulting
Waddell Group	MN - New Brighton	Medical Device Consulting