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Text Content

 * FR
 * EN


 * HOME
 * SERVICES
 * GLOBAL
 * OUR CLIENTS
 * ABOUT US
 * CAREERS
 * CONTACT US




OUR CLIENTS

JSS Medical Research, as an international mid-tier niche CRO, is large enough,
yet nimble enough, to work with a diverse group of clients including global
pharmaceutical, biotechnology, medical device and nutraceutical companies.
Biotechnology companies rely on the company's knowledgeable project teams, and
its customer-centric and flexible approach, to successfully conduct their
critical early phase trials, while pharmaceutical companies can leverage its
niche post-marketing service offerings.


GLOBAL

JSS Medical Research has evolved from a local Canadian CRO (Contract Research
Organization) to an international full service CRO with study involvement in
over 21 countries. Through our corporate head office in Montreal (Canada), our
regional offices in Bogotá (Colombia), Faridabad (India), Warsaw (Poland), as
well as our global network of partners, JSS Medical Research conducts clinical
research in North America, Latin America, Europe, the Middle East, and Asia.


REGIONAL

Our expansion into India, Colombia and Poland enables us to provide our services
to large pharmaceutical clients, and their regional affiliates, in the emerging
Indian and Latin American markets, as well as the established European markets.
For our biotech clients, our expansion has provided them with access to
academics, key opinion leaders, and investigators. This facilitates the
completion of their clinical development programs and helps them gain access to
these important markets.


PEOPLE

Our success depends on the quality of our people. JSS Medical Research has the
necessary critical mass of highly trained professionals from North America,
Latin America, Asia-Pacific, and Europe. Our customer-centric approach allows us
to provide our clients with the highest quality services covering all the
scientific and operational aspects of clinical research.


OUR CLIENTS

JSS Medical Research, as an international mid-tier niche CRO, is large enough,
yet nimble enough, to work with a diverse group of clients including global
pharmaceutical, biotechnology, medical device and nutraceutical companies.
Biotechnology companies rely on the company's knowledgeable project teams, and
its customer-centric and flexible approach, to successfully conduct their
critical early phase trials, while pharmaceutical companies can leverage its
niche post-marketing service offerings.


GLOBAL

JSS Medical Research has evolved from a local Canadian CRO (Contract Research
Organization) to an international full service CRO with study involvement in
over 21 countries. Through our corporate head office in Montreal (Canada), our
regional offices in Bogotá (Colombia), Faridabad (India), Warsaw (Poland), as
well as our global network of partners, JSS Medical Research conducts clinical
research in North America, Latin America, Europe, the Middle East, and Asia.



GLOBAL

REGIONAL

PEOPLE

OUR CLIENTS


RESPONSIVE

We offer creative solutions. You can count on us.


RELIABLE

Our clients think so. They keep coming back.


RESULTS

What you're looking for. What we deliver.


VISIT GD3 AT BOOTH 637 AT THE ASM MICROBE JUNE 13-17 ATLANTA, GA





OUR SERVICES

JSS Medical Research is a full service clinical research organization (CRO) with
strong academic affiliations offering a wide range of services internationally.
One of our distinguishing attributes is our methodological knowledge and
expertise in the design and execution of clinical studies. These include all
phases of development such as Phase I, II and III, and post-approval studies.
The breadth of our experience enables our clients to collaborate with the same
partner throughout the product lifecycle.




 * Clinical Trials
 * Market Access & HEOR
 * Consulting
 * Biostatistics and Medical Writing
 * Insourcing
 * Additional Services


THE JSS TEAM PROVIDES CLIENTS WITH A FLEXIBLE, BEST-IN-CLASS APPROACH TO IMPROVE
CYCLE TIMES, ATTENUATE COSTS AND REDUCE RISKS.


CLINICAL PHASE I-III


EXPERIENCE IN PHASE I-III CLINICAL TRIALS RANGING FROM SMALL TO LARGE COMPLEX
MULTINATIONAL PROJECTS.


CLIENTS BENEFIT FROM THE PLANNING, EXECUTION AND PROACTIVE MANAGEMENT OF
CLINICAL PROGRAMS DESIGNED TO SUCCEED.

Phase I
Phase II
Phase III-IIIb
Medical Devices


LATE & POST-APPROVAL PHASE


POST-APPROVAL OBJECTIVES CAN EASILY BE ATTAINED BY CAREFUL DESIGN AND EXECUTION.

Phase IV
PMOS
RWE
Chart Review
Registries
Database Analysis
Epidemiological Surveys

LITERATURE REVIEW

Extensive literature reviews can be conducted which encompass country-specific
literature databases in addition to the standard medical literature databases.
Systematic reviews of literature are also available should the client require a
well-defined, in-depth, structured process adequate for publication.



MEDICAL WRITING- PHARMAECONOMIC REPORTS AND MEDICAL SUMMARIES

Our specialization in economic modelling combined with our clinical authorship
experience (over 150 manuscripts published by the JSS team with a 90% acceptance
rate) places us in a unique position to produce high quality health economic
reports in an elegant manner with the ability to convey the desired value
message simply and efficiently.



BUDGET IMPACT ANALYSIS

We possess abundant experience building the best-in-class budget impact models.
Additionally, we adapt existing models to different countries and regions. They
can be individually tailored to a specific subpopulation or healthcare system
based on the client’s needs.



CREATION AND ADAPTATION OF COST-EFFECTIVENESS MODELS

We are capable of building and adapting cost-effectiveness models to different
countries and regions. They can be individually tailored to a specific audience,
subpopulation or healthcare system based on the client’s needs.



GRAPHICAL USER INTERFACE

JSS’ strategic partnership with health economics graphical user interface
experts allow us to provide highly customized web-based platforms for budget
impact models. This equips the client with an easy method of sharing complex
health economic models in an efficient, aesthetically-pleasing manner with
stakeholders across the globe.



REIMBURSEMENT SUBMISSION PREPARATION

We prepare submissions for drug and device evaluation to reimbursement
authorities around the globe. This includes collecting and synthesizing all
relevant publications, data, pharmacoeconomic evaluations and clinical summaries
in the preferred format as well as completing all specific submission forms. For
medical devices and products sold in hospitals, submissions tailored to
hospitals and other decision-makers are performed.



VALIDATION SESSION AND PANEL MEETINGS

Our recruitment strategy has been vital in the successful addition of valuable
key opinion leaders or former decision-makers to our projects. We have a breadth
of experience ranging from efficient one-on-one validation sessions via web
conferencing systems to forming advisory boards to simultaneously engage
stakeholders from across the globe in one face-to-face panel meeting. Our
organizational ability permits us to successfully execute meetings of various
magnitudes to match the client’s needs.



LITERATURE REVIEW

Extensive literature reviews can be conducted which encompass country-specific
literature databases in addition to the standard medical literature databases.
Systematic reviews of literature are also available should the client require a
well-defined, in-depth, structured process adequate for publication.



CONSULTING

We have knowledgeable leaders who perform assessments and provide support during
in-person meetings with stakeholders in a variety of languages. Our team
possesses a combination of graduate-level scientific training, experience in
multinational pharmaceutical companies and health technology assessment
organizations. We can offer a client-facing individual who can provide strategic
positioning with or without the use of highly experienced and specialized
strategic partners.


CONSULTING


AS A FULLY INTERGRATED CRO, WE OFFER A COMPLETE RANGE OF SERVICES INCLUDING
CONSULTATION SERVICES.

INVESTIGATOR-INITIATED STUDIES



IN-SOURCING MANDATES



PROJECT MANAGERS

RESEARCH ASSOCIATES/ASSISTANTS

EPIDEMIOLOGY & BIOSTATS COURSES




DEMYSTIFYING STATISTICS PART I

DEMYSTIFYING STATISTICS PART II

THE ARCHITECTURE OF CLINICAL RESEARCH

POST APPROVAL RESEARCH

HEALTH ECONOMICS AND OUTCOME RESEARCH MADE SIMPLE

REVIEW, CRITIQUE AND SYNTHESIS OF THE LITERATURE

CUSTOMIZED COURSES

CLINICAL RESEARCH CONSULTING



REGULATORY

CLINICAL DEVELOPMENT PLAN

STUDY DESIGN

NEEDS ASSESSMENT

PROTOCOL DEVELOPMENT

REGULATORY CONSULTING (HC,FDA,EMEA)

QA SERVICES



COMPLIANCE CONSULTING

SOP DEVELOPMENT

AUDITING

SOFTWARE VALIDATION



GCP TRAINING



GENERAL ICH-GCP

ICH-GCP FOR INVESTIGATORS




BIOSTATISTICS

OUR EXPERIENCED BIOSTATISTICIANS AND STATISTICAL PROGRAMMERS PROVIDE CUTTING
EDGE ANALYSES AND INSIGHTS TO SPONSORS

ANALYSIS DATASET GENERATION



TABLES, FIGURES AND LISTINGS DEVELOPMENT



SAMPLE SIZE CALCULATIONS



ADVANCED BIOSTATISTICS

Multivariate analyses, Repeated measures analyses, Decision trees/recursive
partitioning, Simulation, PK/PD, Other

EPIDEMIOLOGICAL EXPERTISE FOR POST-APPROVAL STUDIES



CDISC SDTM & ADAM MAPPING / PROGRAMMING, AND DEVELOPMENT OF DEFINE.XML



VERIFICATION / QUALITY CONTROL / VALIDATION OF STATISTICAL PROGRAMMING



SAS MACRO DEVELOPMENT


Biostatistics Experience


MEDICAL WRITING


WHETHER RELATED TO EARLY-PHASE OR POST-APPROVAL STUDIES, OUR MEDICAL WRITING
EXPERTS DELIVER QUALITY DOCUMENTS THAT ARE CLEAR, CONCISE, SCIENTIFICALLY
ACCURATE, AND COMPLIANT WITH REGULATIONS, INDUSTRY STANDARDS AND THE SPONSOR’S
INTERNAL GUIDANCE.


OUR MEDICAL WRITERS HAVE EXPERIENCE IN A WIDE RANGE OF INDICATIONS & THERAPEUTIC
AREAS, STUDY DESIGNS, AND MEDICAL WRITING DELIVERABLES, AS WELL AS A PROVEN
PUBLICATION TRACK-RECORD.


Medical Writing Experience


INSOURCING

JSS performs insource services with highly qualified, trained and educated
personnel knowledgeable in ICH and GCP, varied therapeutic areas, applicable
regulatory requirements and pharmacovigilance expertise.




CLINICAL DEVELOPMENT PLAN

The JSS Clinical Development Team can offer consultation and advice on the
strategic path of your clinical study accross many therapeutic areas. This
includes early and late phase development for drugs, medical devices and
nutraceuticals.

STRATEGIC ASSESSMENTS

RISK MANAGEMENT

PATIENT REPORTED OUTCOMES

LITERATURE REVIEW

ADVANCED BIOSTATISTICS AND RESCUE ANALYSIS


JSS MEDICAL RESEARCH: EVOLUTION OF CLINICAL EPIDEMIOLOGY – BEHIND THE SCENES ON
PBS TELEVISION





GLOBAL COVERAGE

JSS offers global coverage with offices in all major continents to deliver
consistently excellent operations with full-time permanent and locally-based
staff. This allows us to execute studies that meet global quality standards
around the world.



Read More



JSS MEDICAL RESEARCH




COMMITMENT TO SCIENTIFIC EXCELLENCE TO SUPPORT THE APPROVAL AND REIMBURSEMENT OF
LIFE SAVING THERAPIES

OUR CLIENTS

JSS Medical Research provides comprehensive clinical trial management services,
from study design to publication of results, in Phase I-IV trials across a broad
range of therapeutic areas to the global pharmaceutical, biotechnology, medical
device and nutraceutical industries.

Read More

ABOUT US

Mission: To conduct health research recognized as the standard of excellence.
Vision: To link industry, academia, regulatory authorities, payers, and patients
through our scientific foundation.
Values: Accountability, responsiveness, results-oriented, teamwork, respect, and
reliability.

Meet our Executive Team


STAY UP TO DATE ON EVERYTHING HAPPENING AT JSS




OUR LATEST NEWS

Please take note that: JSS will be attending BIO 2022 in San Diego from June
12‑16
It will be a pleasure to receive your Visit at the PAVILLION DU QUÉBEC booth
EX‑4323

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GLOBAL HEADQUARTERS

9400 Henri-Bourassa W, St-Laurent (Montreal), Quebec H4S 1N8

+1 514-934-6116 +1 866-934-6116

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© 2023 JSS Medical Research. All rights reserved.
 * HOME
 * SERVICES
 * GLOBAL
 * OUR CLIENTS
 * ABOUT US
 * CAREERS
 * CONTACT US


🎉WELCOME TO JSS MEDICAL RESEARCH! 🎉


ARE YOU SEARCHING FOR A POWERHOUSE PARTNER IN PRODUCT DEVELOPMENT? LOOK NO
FURTHER!


🌎 As a globally recognized Canadian-based CRO, we've got a world of experience
under our belt. Over the past decade, we've navigated high-volume studies
involving over 500,000 patients across 8,500 sites worldwide. You read that
right - half a million patients!

🎯 With a proven track record across a broad spectrum of therapeutic areas from
Oncology to Orthopedics, Infectious Diseases to Immunology, and everything in
between, we've got you covered!

🚀 Our dynamic team is always ready to adapt and respond swiftly to meet the
evolving needs of regulatory authorities and healthcare providers. We're in it
to win it, from Phase I to Phase IV of clinical trials.

🔬 We've got agreements with top-tier hospital sites and research centers across
the globe and have mastered the art of remote and risk-based monitoring
methodologies.

💪 Choose JSS and get ready to turbocharge your product development with a
dedicated, agile team that brings a wealth of knowledge, global reach, and
innovative approaches to the table.

Join us on a journey to successful medical research! 🚀🌟