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TIME IS OF THE ESSENCE IN DRUG DEVELOPMENT.
CONTACT THE QPS BUSINESS DEVELOPMENT TEAM TODAY!
CALL +1 512 350 2827 EMAIL infobd@qps.com
QPS IS A GLOBAL CRO WITH DIVERSE
CAPABILITIES THAT OFFERS END TO
END DRUG DEVELOPMENT SERVICES.
Partnering with QPS for a well-conceived
and executed IND-enabling preclinical
program will provide you with a detailed
assessment of your drug candidate
and the most agile, flexible and timely
pathway to filing an IND.
A flexible approach to
IND-enabling
Preclinical
Studies
f Your proposed non-clinical
plan including proof of concept
studies, pharmacology and
ADME studies, and toxicology/
safety program will be
analyzed in depth
	
f Your proposed non-clinical
plan will be reviewed to
identify deficiencies and
potential roadblocks and
hurdles and whenever possible
solutions identified
	
f Timelines for preclinical
development of your overall
and individual programs will
be mapped out and preclinical
development objectives and
crucial milestones will be
confirmed
www.qps.com	 infobd@qps.com +1 512-350-2827
Why perform your IND-enabling preclinical
studies at QPS?
Before we begin executing your IND-enabling preclinical
program, you will receive strategic review and advice
on the design and execution of your ADME and
pharmacology-toxicology studies:
Operational
Strengths:
	
f ADME scientists and
toxicologists with extensive
industry and CRO experience
allow for optimal planning
and execution of ADME and
pharmacology-toxicology
studies
	
f State-of-the-art ADME,
toxicology and bioanalytical
facilities
	
f Rapid execution and
completion of all preclinical
studies required for IND
submission
	
f All studies will be carefully
monitored and every phase of
the studies critically assessed
for scientific rigor and quality
	
f Fast turnaround on high-
quality non-clinical study
reports
	
f Extensive experience in the
preparation of ADME and
pharmacology-toxicology
sections of IND submissions
	
f An experienced program
manager will be assigned
to ensure rigorous program
oversight
Scientific/Regulatory
Pre-IND/IND Support:
	
f ADME scientists and
toxicologists with extensive
industry and CRO experience
allow for optimal planning
and execution of ADME and
pharmacology-toxicology
studies
	
f Review and gap analysis of
available data & preclinical
development plans
	
f Advice on the design and
timing of ADME, safety
pharmacology, and toxicology
studies
	
f Provide expert advice on ADME
and pharmacology-toxicology
issues associated with a broad
range of therapeutic areas
	
f Rapid completion of the ADME
and pharmacology-toxicology
sections of the IND to enable
client to file the IND in a timely
manner
During execution of your IND-enabling program you
will benefit from QPS’s operational strengths, strong
scientific/regulatory pre-IND/IND support, and drug
development experience.
What are the Benefits of Working with QPS?
AGILITY. FLEXIBILITY. SPEED
WWW.QPS.COM
Fargo, ND, USA
Dermal and Transdermal
Research Laboratory (DTRL)
Groningen and Leeuwarden,
The Netherlands
Bioanalysis (BA)
Clinical Research Services (CRS)
Translational Medicine (TLM)
Suzhou and Shanghai,
China
Bioanalysis (BA)
Clinical Research Services (CRS)
Miami, FL, USA
Clinical Research
Services (CRS)
Hyderabad, India
Bioanalysis (BA)
Clinical Research
Services (CRS)
Taipei, Taiwan
Bioanalysis (BA)
Clinical Research Services (CRS)
Toxicology (TOX)
Newark, DE, USA
Bioanalysis (BA)
Clinical Research Services (CRS)
DMPK
Translational Medicine (TLM)
Global Headquarters for
QPS Holdings LLC
Graz, Austria
Clinical Research Services (CRS)
DMPK
Histology Services
Neuropharmacology
Rare Disease
Rodent Biobank
Springfield, MO, USA
Clinical Research
Services (CRS)
QPS is a Global CRO
with locations around the world
to serve the evolving needs of the
Pharmaceutical and Biotech industries
IND-enabling
Preclinical
Studies
CALL +1 512 350 2827
EMAIL infobd@qps.com

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QPS IND Enabling Preclinical Studies

  • 1. TIME IS OF THE ESSENCE IN DRUG DEVELOPMENT. CONTACT THE QPS BUSINESS DEVELOPMENT TEAM TODAY! CALL +1 512 350 2827 EMAIL infobd@qps.com QPS IS A GLOBAL CRO WITH DIVERSE CAPABILITIES THAT OFFERS END TO END DRUG DEVELOPMENT SERVICES. Partnering with QPS for a well-conceived and executed IND-enabling preclinical program will provide you with a detailed assessment of your drug candidate and the most agile, flexible and timely pathway to filing an IND. A flexible approach to IND-enabling Preclinical Studies
  • 2. f Your proposed non-clinical plan including proof of concept studies, pharmacology and ADME studies, and toxicology/ safety program will be analyzed in depth f Your proposed non-clinical plan will be reviewed to identify deficiencies and potential roadblocks and hurdles and whenever possible solutions identified f Timelines for preclinical development of your overall and individual programs will be mapped out and preclinical development objectives and crucial milestones will be confirmed www.qps.com infobd@qps.com +1 512-350-2827 Why perform your IND-enabling preclinical studies at QPS? Before we begin executing your IND-enabling preclinical program, you will receive strategic review and advice on the design and execution of your ADME and pharmacology-toxicology studies:
  • 3. Operational Strengths: f ADME scientists and toxicologists with extensive industry and CRO experience allow for optimal planning and execution of ADME and pharmacology-toxicology studies f State-of-the-art ADME, toxicology and bioanalytical facilities f Rapid execution and completion of all preclinical studies required for IND submission f All studies will be carefully monitored and every phase of the studies critically assessed for scientific rigor and quality f Fast turnaround on high- quality non-clinical study reports f Extensive experience in the preparation of ADME and pharmacology-toxicology sections of IND submissions f An experienced program manager will be assigned to ensure rigorous program oversight Scientific/Regulatory Pre-IND/IND Support: f ADME scientists and toxicologists with extensive industry and CRO experience allow for optimal planning and execution of ADME and pharmacology-toxicology studies f Review and gap analysis of available data & preclinical development plans f Advice on the design and timing of ADME, safety pharmacology, and toxicology studies f Provide expert advice on ADME and pharmacology-toxicology issues associated with a broad range of therapeutic areas f Rapid completion of the ADME and pharmacology-toxicology sections of the IND to enable client to file the IND in a timely manner During execution of your IND-enabling program you will benefit from QPS’s operational strengths, strong scientific/regulatory pre-IND/IND support, and drug development experience. What are the Benefits of Working with QPS? AGILITY. FLEXIBILITY. SPEED
  • 4. WWW.QPS.COM Fargo, ND, USA Dermal and Transdermal Research Laboratory (DTRL) Groningen and Leeuwarden, The Netherlands Bioanalysis (BA) Clinical Research Services (CRS) Translational Medicine (TLM) Suzhou and Shanghai, China Bioanalysis (BA) Clinical Research Services (CRS) Miami, FL, USA Clinical Research Services (CRS) Hyderabad, India Bioanalysis (BA) Clinical Research Services (CRS) Taipei, Taiwan Bioanalysis (BA) Clinical Research Services (CRS) Toxicology (TOX) Newark, DE, USA Bioanalysis (BA) Clinical Research Services (CRS) DMPK Translational Medicine (TLM) Global Headquarters for QPS Holdings LLC Graz, Austria Clinical Research Services (CRS) DMPK Histology Services Neuropharmacology Rare Disease Rodent Biobank Springfield, MO, USA Clinical Research Services (CRS) QPS is a Global CRO with locations around the world to serve the evolving needs of the Pharmaceutical and Biotech industries IND-enabling Preclinical Studies CALL +1 512 350 2827 EMAIL infobd@qps.com