JCS EDITORIAL CALENDAR 2018 · 2019-01-29 · reviewed. Supported by a team of industry experts,...
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MEDIA INFORMATION CONTACT [email protected] T + 44(0)207 2372036 JCS – Journal for Clinical Studies is peer reviewed. Supported by a team of industry experts, JCS brings you contemporary and authoritative articles which will guide the industry in the best practice in regulatory issues, market analysis, drug discovery, development, drug design, clinical research, data analysis, safety and efficacy, recruitment and retention, laboratories, analytical testing, custom and contract manufacturing, primary and secondary packaging and logistics and supply chain management. Please visit our website www.jforcs.com, to view our Peer review protocol, and author guidelines. EDITORIAL SECTIONS Watch Pages Regulatory Market Report Therapeutics Technology Supplies FDA & EMA Watch Page - Latest guidelines from FDA & EMA on foreign clinical Trials Market Report Section will also carry features on Ethics Committees, IRBs, Ethics Committee Approval, Investigator Registration, Patient Empowerment, Informed Consent, Patient Reviews & Aftercare, Patient Recruitment & Retention Strategies, and Investigator Payments. JCS EDITORIAL CALENDAR 2018
Transcript of JCS EDITORIAL CALENDAR 2018 · 2019-01-29 · reviewed. Supported by a team of industry experts,...
MEDIA INFORMATION
CONTACT [email protected] T + 44(0)207 2372036
JCS – Journal for Clinical Studies is peer
reviewed. Supported by a team of industry
experts, JCS brings you contemporary and
authoritative articles which will guide the
industry in the best practice in regulatory issues,
market analysis, drug discovery, development,
drug design, clinical research, data analysis,
safety and efficacy, recruitment and retention,
laboratories, analytical testing, custom and
contract manufacturing, primary and secondary
packaging and logistics and supply chain
management.
Please visit our website www.jforcs.com, to view our
Peer review protocol, and author guidelines.
EDITORIAL SECTIONS
Watch Pages Regulatory
Market Report Therapeutics
Technology Supplies
FDA & EMA Watch Page - Latest guidelines from
FDA & EMA on foreign clinical Trials
Market Report Section will also carry features on
Ethics Committees, IRBs, Ethics Committee
Approval, Investigator Registration, Patient
Empowerment, Informed Consent, Patient
Reviews & Aftercare, Patient Recruitment &
Retention Strategies, and Investigator Payments.
JCS EDITORIAL CALENDAR 2018
EDITORIAL CALENDAR 2018
CONTACT [email protected] +44 (0) 207 2372036
For Events & Conferences attended by JCS, please visit our website at – www.jforcs.com
Watch Pages > FDA & EMA* > Logistics
> Oncology > Cardiovascular Device
> Cardiovascular Therapeutics > Personalised Medicine
> Insurance > E Clinical
> CNS > General Medicine
Market Evaluation > Australia & New Zealand > India
> China
Therapeutic Areas > Alzheimer’s > Endocrine & Metabolic
> Metabolic Stress > Bronchodilation
> Renal & Hepatic Impairment > Diabetes
> Treating lung disorders > Orphan Diseases
Features > Risk-based monitoring > ABPM
> Holter monitoring > Comparator Sourcing
> Translation Services > Clinical Trials Directive
> Patient Facing Clinical Trials Regulatory Update > Investigator Payments
>Subject – Travel &Reimbursement > Ambulatory Services
> Late Phase Cl inical Trials
> Outsourcing trends in medical device & diagnostics clinical trials
> The growing identification of combinatorial chemistry technology
> Regulatory initiatives fostering demand for pharmacogenomics technology
> Proteomics in anticancer drug discovery
> Strategic alignment of study objectives and endpoints to drive value and fill data gaps
> Medical Affairs approach to developing and implementing clinical studies (Phase I to IV)
> Target validation, efficacy, and safety studies
Volume 10 Issue 1 - January 2018 Submission Deadline - 10th December 2017
Special Subsection
Risk Based Monitoring
EDITORIAL CALENDAR 2018
CONTACT [email protected] +44 (0) 207 2372036
For Events & Conferences attended by JCS, please visit our website at – www.jforcs.com
Watch Pages > FDA & EMA* > Logistics
> Oncology > Cardiovascular Device
> Cardiovascular Therapeutics > Personalised Medicine
> Insurance > E Clinical
> CNS > Pediatric
Market Evaluation > ASEAN Country Focus > Singapore
> Japan > Thailand
> China > South Korea
> Malaysia
Therapeutic Areas > Schizophrenia > Cardiovascular / Metabolic
> Food Borne > Bacterial & Mycotic
> Obesity & Metabolic > Orthopedic
Features > QTc Prolongation/Cardiac Safety > PK/PD Studies
> BIO Equivalence & Bio – Availability > Pharmacovigilance & Risk Management
> Temperature & Time Sensitive Logistics > Clinical Trials Logistics
> Equipment Transportation & Customs > Clinical Trials Reimbursement
> Site Management > Clinical Trials Packaging & Labeling
> Human protein microarray for various protein analysis
> Avoiding hidden costs in conducting clinical trials
> Trial Design
> Site Selection
> Understanding the challenges in designing and executing clinical trials for screening tests
> Comparing the difference between clinical trials for screening tests and clinical trials for traditional
medical devices/in-vitro diagnostic tests
Volume 10 Issue 2 – March 2018 Submission Deadline - 10th February 2018
Special Subsection
Clinical Trials Logistics
IMP Supplies
Cold/Cool Chain Management
EDITORIAL CALENDAR 2018
CONTACT [email protected] +44 (0) 207 2372036
For Events & Conferences attended by JCS, please visit our website at – www.jforcs.com
Watch Pages > FDA & EMA* > Logistics
> Oncology > Cardiovascular Device
> Cardiovascular Therapeutics > Personalised Medicine
> Insurance > E Clinical
> CNS > General Medicine
Market Evaluation > USA > Canada
> Latin America
Therapeutic Areas > Ebola > Immunology/Hematology
> Cardiology > Pediatrics
> Gastroenteritis > Vaccines
> Oncology > Women’s Health
> CNS disorders > Orphan Diseases
Features > Preclinical > Archival
> Imaging Labs/ Central Labs/ ECG & Core Labs > Calibration/Validation
> Recruitment & Retention > Translation Systems
> EDC – Data capture & Evaluation > IMP Supplies
> Temperature Controlled > Named Patient Programme
> Time/ Temp. Data Logging & Monitoring > Packaging & Logistics
> Pharmacogenomics and Personalised Medicine
> Late stage research (II-IV)
– the unique challenges of the post-approval environment – customising study design
> Patient recruitment and retention in clinical development
> Mergers and acquisitions of pharma and biopharma companies
> How the focus on personalised medicine is shaping the industry
Volume 10 Issue 3 – May 2018 Submission Deadline – 10th April 2018
Special Subsection
Patient Recruitment & Retention
Site Selection & Feasibility
EDITORIAL CALENDAR 2018
CONTACT [email protected] +44 (0) 207 2372036
For Events & Conferences attended by JCS, please visit our website at – www.jforcs.com
Watch Pages > FDA & EMA* > Logistics
> Oncology > Cardiovascular Device
> Cardiovascular Therapeutics > Personalised Medicine
> Insurance > E Clinical
> CNS > Oncology
Market Evaluation > Sub Saharan Africa > Latin America
> South Africa
Therapeutic Areas > Transplant Research > Dermatology
> Nutrition/Malnutrition > Oncology in Pediatrics
> Ophthalmology > Respiratory (COPD)
> Inflammatory diseases > Rare Diseases
Features > Trial Partners & CROs > Global Central Labs
> Imaging & Core Lab > Biosimilars
> Biotech & Clinical Research > Remote Data Acquisition/Analysis
> Preclinical & Phase I > Proof of Concept
> Translation Services > RIB & Ethics Review Boards
> Medical Devices > Patient Recruitment & Retention
> Globalising clinical trials > Patient centricity in clinical trials
> Data management/biometrics/medical writing
> Assessing complexity of study design and matching to systems based on efficiency and cost-effectiveness
> Evaluating needs and available in-house resources for managing data and regulatory documentation
> Patient centricity in clinical trials – the FDAs Patient-Focused Drug Development
> Use of investigative sites in Central & Eastern Europe for clinical studies
> The new EU clinical trials regulations
Volume 10 Issue 4 – July 2018 Submission Deadline – 10th June 2018
Special Subsection
Mobile Technology in CT
ePRO & BOYD
EDITORIAL CALENDAR 2018
CONTACT [email protected] +44 (0) 207 2372036
For Events & Conferences attended by JCS, please visit our website at – www.jforcs.com
Watch Pages > FDA & EMA* > Logistics
> Oncology > Cardiovascular Device
> Cardiovascular Therapeutics > Personalised Medicine
> Insurance > E Clinical
> CNS > General Medicine
Market Evaluation > Russia > CIS States
> CEE States > Central Europe
> Scandinavia
Therapeutic Areas > Pain > Cardiovascular
> Cardiovascular safety > Diabetes
> Renal & Hepatic Impairment > Respiratory
> Cervical Cancer > Cancer/Immunotherapy
Features > Clinical Trials Packaging/Materials Management > Medical Devices & Trials
> IVRS/IWRS > eCTD
> Clinical Trials > Strategies & Innovation, Phase I – IV
> CRAs Training & Evaluation > CDISC/CDASH
> Pharmacovigilance & Drug Safety > How personalized medicine shapes the industry
> Reducing development timelines and associated costs of clinical research
> Testing usability for investigational site staff and sponsor data/regulatory documentation management
> EDC builds: Outsourcing or use of in-house resources (impacted by study complexity, system capabilities and costs)
> Increasing the industry Sustainability by using patient inspired solutions
> The promise of reporting systems in patient safety
> Emerging role of bioinformatics tools in the evolution of clinical research
Volume 10 Issue 5 – September 2018 Submission Deadline – 10th August 2018
Special Subsection
Cardiovascular Safety
Cardiovascular Device Safety
Central Labs, ECG & Core Labs
EDITORIAL CALENDAR 2018
CONTACT [email protected] +44 (0) 207 2372036
For Events & Conferences attended by JCS, please visit our website at – www.jforcs.com
Watch Pages > FDA & EMA* > Logistics
> Oncology > Cardiovascular Device
> Cardiovascular Therapeutics > Personalised Medicine
> Insurance > E Clinical
> CNS > Pediatrics
Market Evaluation > Turkey > Middle East
> North Africa
Therapeutic Areas > Diabetes > Reproductive & Maternal Health
> Malaria > Pediatric
> Overcoming clinical challenges when conducting respiratory studies
Features > Analytical Methods & Validation > Imaging
> EDC & Information Technology > ePRO / BOYD / eCOA
> SMO & the I nves t i ga t i ve Site > Customs Regulations
> Remote Patient Monitoring > Logistics – Hazardous Cargo
> The integrated clinical enterprise
> The impact of the empowered patient on medical research (research design, protocol feasibility, communication of study
information)
> Accomplishing quality study data to improve reimbursements and increase market access
> Planning a global trial
> Discussing the financial challenge to run a PMA study
> The importance of Subject Recruitment and Retention to clinical trial success
> Lessons learned and ways forward
> FDA` Post-marketing safety surveillance program for drug and therapeutic biologic products
Volume 10 Issue 6 – November 2018 Submission Deadline – 10th October 2018
Special Subsection
Vaccine Development
Oncology Clinical Trials
CONTACT Journal for Clinical studies B202.2, Tower Bridge Business Complex 100 Clements Road London – SE1 5RT T: +44 (0) 207 2372036 E: [email protected] W: www.jforcs.com Advertising: Mark Barker [email protected]
Editorial: Virginia Toteva [email protected]
Production: Cecilia Stroe [email protected]
Subscriptions Martin Wright [email protected]
