Dashboard (Affiliates)

My Requests
18 Pending
My Requests
9 Approved
Next Validation Date
12th July 2022
Next P&R Review
30th April 2022
Current Price Requests
My Approvals Needed
Date Created Request Title Requested By Deadline
16/02/2022 Lorem ipsum dolor sit pmet Request Personname 09/03/2022
16/02/2022 Vis erat denique in, dicunt prodesse Request Personname 14/03/2022
16/02/2022 Vis erat denique in, dicunt prodesse Request Personname 14/03/2022
My Requests Needing Approval
Date Created Request Title Action With Deadline
16/02/2022 Sit meis deleniti eu, pri vidit meliore docendi ut Action Personname 09/03/2022
02/03/2022 An eum erat animal commodo Action Personname
Another Personname
10/03/2022
31/12/2022 Sed pulvinar, massa vitae interdum pulvinar Action Personname 05/04/2022
31/12/2022 Sed pulvinar, massa vitae interdum pulvinar Action Personname 05/04/2022
IRP Map SAMPLE
Market Access News
Date Title Author
23/12/2022 LAST WEEK IN REVIEW Dhriti.Gupta@Eversana.com
22/12/2022 ICER Publishes Draft Evidence Report Evaluating Emerging Therapies for Alzheimer’s Disease raechel.pusateri@eversana.com
22/12/2022 In Formal Request, Alzheimer’s Association Asks CMS to Reconsider Aduhelm Coverage Decision raechel.pusateri@eversana.com
22/12/2022 NPPA Finalizes Framework for Suo Moto Corrections in Notified Prices to Improve Pricing Process Dhriti.Gupta@Eversana.com
22/12/2022 New Zealand to Source Alternative Diabetes Treatment in Response to Global Trulicity Shortage raechel.pusateri@eversana.com
22/12/2022 Happy Holidays & Warm Wishes for a Healthy New Year! anna.smith@eversana.com
22/12/2022 India's NPPA Fixes Ceiling Price of 12 Formulations Under DPCO, 2013 Dhriti.Gupta@Eversana.com
22/12/2022 Brazilian Health System and Novartis Agree to Innovative Payment Model to Cover Cost of Zolgensma raechel.pusateri@eversana.com
22/12/2022 FDA Oks Lupin to Market Generic Version of Briviact Dhriti.Gupta@Eversana.com
22/12/2022 EU Backs 2 AZ Oncology Drugs anna.smith@eversana.com
22/12/2022 ICER Issues Final Report Assessing Clinical Effectiveness and Value of Gene Therapies Targeting Hemophilia raechel.pusateri@eversana.com
22/12/2022 EUnetHTA 21 Publishes 5 More Deliverables anna.smith@eversana.com
22/12/2022 FDA Approves Roche’s Actemra for Hospitalized COVID-19 Patients anna.smith@eversana.com
22/12/2022 EC Grants ODD to Henlius’ Hansizhuang anna.smith@eversana.com
22/12/2022 Generic Association Celebrates Lauterbach for “Finally” Tackling Supply Issues anna.smith@eversana.com
22/12/2022 Over 4 Crores Health Cards Digitized in India Under ABDM Dhriti.Gupta@Eversana.com
21/12/2022 India's NPPA Revises Ceiling Price of 107 Formulations Under DPCO, 2013 Dhriti.Gupta@Eversana.com
21/12/2022 India's NPPA Fixes Ceiling Price of 10 Formulations Under DPCO, 2013 Dhriti.Gupta@Eversana.com
21/12/2022 Final “Yes” from Chamber Paves Way for AIFA Reform anna.smith@eversana.com
21/12/2022 ICER Issues Revised Evidence Report Evaluating Multiple Sclerosis Treatments raechel.pusateri@eversana.com
21/12/2022 U.S. Spending Package Addresses Accelerated Approval, Other Health Care Reforms raechel.pusateri@eversana.com
21/12/2022 Kite Pharma Announces Acquisition of Tmunity Therapeutics raechel.pusateri@eversana.com
21/12/2022 EU Approves Zynlonta for R/R DLBCL anna.smith@eversana.com
21/12/2022 Glenmark Launches Novel Triple FDC Teneligliptin with Pioglitazone & Metformin in India Dhriti.Gupta@Eversana.com
21/12/2022 ICER Updates Health-Benefit Price Benchmark for Paxlovid raechel.pusateri@eversana.com
21/12/2022 CSL Behring Selects Orsini Specialty as Hemgenix Distribution Partner raechel.pusateri@eversana.com
21/12/2022 UK MHRA Accepts EQRX’s MAA for Sugemalimab & Chemo Combo to Treat Metastatic NSCLC Dhriti.Gupta@Eversana.com
21/12/2022 After Delays, Ontario to Establish Biosimilar Switching Policy raechel.pusateri@eversana.com
21/12/2022 Japan OKs Breyanzi as 2nd-line R/R Large B-cell Lymphoma Treatment anna.smith@eversana.com
21/12/2022 Egypt to Produce 76 Cancer Drugs Locally in the First Half of 2023 Dhriti.Gupta@Eversana.com
21/12/2022 German Health Minister Announces More Major Changes to System anna.smith@eversana.com
20/12/2022 FDA Approves New Indication for Eagle Pharmaceuticals’ Pemfexy raechel.pusateri@eversana.com
20/12/2022 France Backs Orphan Drug Xenpozyme anna.smith@eversana.com
20/12/2022 Insulin Shortage in Pakistan, Experts Claim of Price Hike Up to 53% Dhriti.Gupta@Eversana.com
20/12/2022 Brazilian Pilot Project Successfully Streamlines Post-registration Requests for Biologics rachel.yalisove@eversana.com
20/12/2022 Catalyst Pharmaceuticals to Purchase U.S. Commercial Rights to Eisai’s Fycompa CIII raechel.pusateri@eversana.com
20/12/2022 Atara’s Ebvallo Receives EC Approval as First EBV+ PTLD Treatment Dhriti.Gupta@Eversana.com
20/12/2022 France Maintains Reimbursement of Remicade for Pediatric Crohn’s anna.smith@eversana.com
20/12/2022 New Zealand Funds Janssen’s Stelara and Remicade rachel.yalisove@eversana.com
20/12/2022 NICE Places Enhertu in CDF for More Advanced Breast Cancer Patients anna.smith@eversana.com
20/12/2022 Ono Collaborates with PrecisionLife to Discover Novel Therapies for CNS Diseases Dhriti.Gupta@Eversana.com
20/12/2022 Eisai, Washington University Collaborate to Create Novel Treatments for Neurodegenerative Disorders Dhriti.Gupta@Eversana.com
20/12/2022 Chuikyo Greenlights FY2023 Off-year Price Revision Rules, Pharma Reacts anna.smith@eversana.com
20/12/2022 Australia Updates Medicines Policy For First Time in More Than 20 Years rachel.yalisove@eversana.com
20/12/2022 EU Approves Enhertu for 2nd Line Treatment of HER2+ Gastric or GEJ Cancer Dhriti.Gupta@Eversana.com
20/12/2022 Daiichi Sankyo Launches Ezharmia in Japan for T-Cell Leukemia-Lymphoma anna.smith@eversana.com
19/12/2022 Sosei Inks Licensing Deal with Lilly in Diabetes & Metabolic Disease anna.smith@eversana.com
19/12/2022 Indian Council of Medical Research to Conduct Research in ‘Therapeutics for Inherited Rare Diseases’ Dhriti.Gupta@Eversana.com
19/12/2022 Korea Reveals ICER Evaluations for First Time in 15 Years rachel.yalisove@eversana.com
19/12/2022 IMC Supports Delay in PMPRB Guideline Implementation rachel.yalisove@eversana.com
19/12/2022 FDA Approves Ferring Pharma’s Gene Therapy for Bladder Cancer raechel.pusateri@eversana.com
19/12/2022 Vraylar Receives FDA Nod for Treatment of Major Depressive Disorder raechel.pusateri@eversana.com
19/12/2022 TLV Includes Farydak in High-cost Protection for Certain MM Patients Luke.Hannaford@Eversana.com
19/12/2022 Sanofi Expands Collaboration With Innate for Natural Killer Cell Therapeutics in Oncology Luke.Hannaford@Eversana.com
19/12/2022 LAST WEEK IN REVIEW Dhriti.Gupta@Eversana.com
19/12/2022 G-BA Gives Orphan Drug Brineura Highest Rating in Latest Meeting anna.smith@eversana.com
19/12/2022 Europe Launches Cross-border Project to Improve Affordability & Accessibility of Innovation anna.smith@eversana.com
19/12/2022 COVID-19 Vaccines Saved Australia’s Economy, Finds New Study rachel.yalisove@eversana.com
19/12/2022 FDA Lifts Partial Clinical Hold for Pediatric Patients in Bluebird Bio Sickle Cell Disease Studies raechel.pusateri@eversana.com
19/12/2022 Shilpa Medicare Launches Capebel 1000mg Dispersible Tablets to Treat Metastatic Breast Cancer in India Dhriti.Gupta@Eversana.com
19/12/2022 Oxford’s Ebola Vaccine Manufactured by Serum Institute India Shipped to Uganda Dhriti.Gupta@Eversana.com
19/12/2022 U.S. Congress Revisits Antimicrobial Netflix Model rachel.yalisove@eversana.com
19/12/2022 Madrigal’s NASH Candidate Achieves Promising Phase 3 Results rachel.yalisove@eversana.com
19/12/2022 France in Favor of Reimbursing Kymriah for Certain Follicular Lymphoma Patients Luke.Hannaford@Eversana.com
19/12/2022 France Backs Keytruda as Adjuvant Treatment for Stage IIB, IIC, or III Melanoma Following Complete Resection Luke.Hannaford@Eversana.com
19/12/2022 Janssen Withdraws EU Application Seeking Approval of Imbruvica for Patients With Untreated MCL Luke.Hannaford@Eversana.com
19/12/2022 Lotus Pharmaceuticals Acquires Eli Lilly’s Cancer Drug Alimta in Taiwan Dhriti.Gupta@Eversana.com
19/12/2022 Prescryptive Health and Eli Lilly to Offer Value-Based Payment Model for Insulin raechel.pusateri@eversana.com
19/12/2022 Attralus Announces Orphan Drug Designation for AT-01 in Europe raechel.pusateri@eversana.com
19/12/2022 FDA Greenlights Glenmark’s Generic Equivalent of Cardene Hypertension Drug Dhriti.Gupta@Eversana.com
19/12/2022 Reata & Lilly Withdraw Drugs from EMA anna.smith@eversana.com
16/12/2022 European Commission Lays Out Further Info on EU Pharmaceutical Strategy anna.smith@eversana.com
16/12/2022 AbbVie Leaves PhRMA & Other Industry Groups rachel.yalisove@eversana.com
16/12/2022 Fimea Publishes Assessment of Vyvgart for Myasthenia Gravis Luke.Hannaford@Eversana.com
16/12/2022 48% Of Listed Products in Japan to Face Price Cuts Under Off-year Revision anna.smith@eversana.com
16/12/2022 ABPI Warns 'Skyrocketing' VPAS Clawback Puts UK Sector at Risk Luke.Hannaford@Eversana.com
16/12/2022 Pakistan’s Health Ministry Seeks Investigation into Non-Opening of LCs Dhriti.Gupta@Eversana.com
16/12/2022 Spanish Association Calls for Direct Collaboration with Health Administrations to Improve Financing of Drugs Luke.Hannaford@Eversana.com
16/12/2022 Fimea Publishes Economic Assessment of Kapruvia for Severe Pruritus Luke.Hannaford@Eversana.com
16/12/2022 CHMP Recommends 5 New Drugs Luke.Hannaford@Eversana.com
16/12/2022 FDA Grants Orphan Drug Designation to Ocugen’s Investigational Rare Retinal Disease Drug raechel.pusateri@eversana.com
16/12/2022 Torrent Pharma Ties Up with BI India to Co-market its Anti-diabetic Drug Dhriti.Gupta@Eversana.com
16/12/2022 Federal Judge Upholds Arkansas State Law Protecting the Use of Contract Pharmacies under 340B raechel.pusateri@eversana.com
16/12/2022 Nexium, Lexapro, Bonviva Face Generic Entry in Japan anna.smith@eversana.com
16/12/2022 France Grants Early Access to Amvuttra for hATTR Amyloidosis Luke.Hannaford@Eversana.com
16/12/2022 New York’s Community Care Health Orgs Brace for Loss in Federal Reimbursement Funding rachel.yalisove@eversana.com
15/12/2022 NHS Director Hails Commercial Deals & VPAS, Despite Industry Concern anna.smith@eversana.com
15/12/2022 TLV Forecasts SEK 2.4B in Savings From Side Agreements in 2022 Luke.Hannaford@Eversana.com
15/12/2022 Takeda Launches Cinryze in India to Treat Rare Genetic Condition Hereditary Angioedema Dhriti.Gupta@Eversana.com
15/12/2022 JB Pharma Inks Deal with Glenmark to Acquire Razel Franchise for India & Nepal Dhriti.Gupta@Eversana.com
15/12/2022 Amid Nationwide Shortage, Alberta, Canada Secures Imported Pain Meds from Turkey rachel.yalisove@eversana.com
15/12/2022 Wales Recommends Votubia for Tuberous Sclerosis Complex Luke.Hannaford@Eversana.com
15/12/2022 EU Backs Sanofi’s Dupixent for Prurigo Nodularis anna.smith@eversana.com
15/12/2022 AEMPS Issues Recommendations to Alleviate Supply Problems with Fibrinolytic Drugs Luke.Hannaford@Eversana.com
15/12/2022 State Prisons Gain Purchase Power for Gilead’s Hep C Drugs rachel.yalisove@eversana.com
15/12/2022 Innovent Biologics and LG Chem Enter License Agreement Regarding Tigulixostat raechel.pusateri@eversana.com
15/12/2022 Angelini Pharma Launches Ontozry in France for Epilepsy Luke.Hannaford@Eversana.com
15/12/2022 50% of EMIG Companies to Reduce Supply to UK in 2022 anna.smith@eversana.com
15/12/2022 FDA Approves Fresenius Biosimilar Referencing Humira raechel.pusateri@eversana.com
15/12/2022 FDA Grants Orphan Drug Designation to PharmaTher’s Ketamine raechel.pusateri@eversana.com
Notifications

This is the task, but I'm not sure how long this is?

By Person Name :: Due DD/MM/YY

This is the task, but I'm not sure how long this is? It could potentially be quite long I guess so lets just see what that looks like.

By Person Name :: Due DD/MM/YY

This is the task, but I'm not sure how long this is?

By Person Name :: Due DD/MM/YY

This is the task, but I'm not sure how long this is?

By Person Name :: Due DD/MM/YY

P&R Questionnaire

??? – Reference Basket of user’s country, and also P&R Forms waiting for validation (although this latter might also / exclusively be in a “Tasks” widget

Country Approval Flow

??? – Steps of the approval flow for their country, including names of approvers at each stage

Report or Chart

??? – mini version of system reports & charts, or custom built – clicking would load full version

Quick Access Reports

??? – a list of reports that the user (or Admin) has chosen to appear on homepage

ID Name Desc
001 Name 1 Info here
002 Name 2 What I need to know
Task Lists
  • Rejected
    Task Number 1

    Last Updated DD/MM/YY

  • Task Number 2

    Last Updated DD/MM/YY

  • Task Number 3

    Last Updated DD/MM/YY

  • Task Number 4

    Last Updated DD/MM/YY

  • Task Number 5

    Last Updated DD/MM/YY

  • Task Number 6

    Last Updated DD/MM/YY

  • Task Number 7

    Last Updated DD/MM/YY

  • Task Number 8

    Last Updated DD/MM/YY

IRP Calendar

??? – Date items from the IRP calendar, filtered by Affiliate(s). 3 months behind, 9 months ahead

Validate Prices

??? – Price Requests due to go live in next two weeks but not yet validated. Also would show when price validation was last done and when due

Exchange Rate
0.0000