№ lp_1_2_02313
File format: docx
Character count: 5821
File size: 175 KB
Invitation to offer document detailing the procurement requirements, framework period, submission process, and compliance obligations for suppliers of Tocilizumab Injection under NHS England.
Year:
2025
Organization:
NHS England, Medicines Procurement and Supply Chain (MPSC)
Type of document:
Invitation to offer / Procurement document
Project title:
NHS National Framework for the supply of Tocilizumab Injection
Offer reference number:
CM/TNS/25/5723
Period of framework:
1 March 2026 to 31 August 2027, with option to extend up to 24 months
Publication date:
7 October 2025
Submission deadline:
5 November 2025, 13:00
Platform for submission:
Atamis / Central Digital Platform
Requirements:
Evergreen assessment, Carbon Reduction Plan, registration on Central Digital Platform
Author / contact:
Katie Noonan, Medicines Procurement Coordinator, NHS England
Region:
United Kingdom
Audience:
Suppliers eligible to participate in NHS procurement
Type of procurement:
Medicines supply
Price: 8 / 10 USD
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The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
2026
Region / City:
Australia
Theme:
Pharmaceutical
Document Type:
Submission for approval
Organization:
PBAC (Pharmaceutical Benefits Advisory Committee)
Author:
Roche Products Pty Ltd
Target Audience:
Medical Practitioners
Effective Period:
Ongoing
Approval Date:
November 2018
Date of Last Revision:
2026
Category / Program:
GENERAL – General Schedule (Code GE)
Prescriber type:
Medical Practitioners
Condition:
Severe active juvenile idiopathic arthritis
PBS Indication:
Severe active juvenile idiopathic arthritis
Treatment phase:
Initial treatment, Continuing treatment
Restriction Level / Method:
Restricted benefit, Authority Required
Clinical criteria:
No more than 16 weeks of treatment allowed under restriction
Prescriber Instructions:
Specific dosage requirements based on patient weight
Comparator:
IV tocilizumab, etanercept, adalimumab
Sponsor hearing:
None
Consumer comments:
None
Clinical trials:
JIGSAW 117 trial
Note:
Year
Year:
2025
Region / City:
USA
Theme:
Cancer treatment, Clinical trials
Document Type:
Side effect table
Organization / Institution:
NCI CIRB
Author:
NCI CIRB
Target Audience:
Research staff, Clinical trial professionals
Approval Date:
N/A
Date of Last Update:
December 5, 2025
Period of Validity:
N/A
Year:
2025
Region / City:
Australia
Topic:
Pharmaceutical submission for drug listing
Document Type:
Pharmaceutical submission
Organization:
Janssen-Cilag Pty Ltd
Author:
Not specified
Target Audience:
Healthcare professionals, regulatory authorities
Validity Period:
Not specified
Approval Date:
Not specified
Date of Changes:
March 2025
Note:
Context
Year:
2026
Region / City:
EMEA
Subject:
Pharmaceutical Information
Document Type:
Product Information
Organization / Institution:
European Medicines Agency
Author:
European Medicines Agency
Target Audience:
Healthcare Professionals, Medical Practitioners
Validity Period:
Not specified
Approval Date:
Not specified
Amendment Date:
Not specified
Year:
2023
Region / City:
Australia
Subject:
Chronic migraine, medicinal product submission
Document type:
Submission for PBS listing
Organization:
Novartis Pharmaceuticals Australia Pty. Limited
Author:
Not specified
Target audience:
Health professionals, pharmaceutical regulatory bodies
Period of validity:
Not specified
Date of approval:
2 July 2018
Date of amendments:
November 2023
Year:
2024
Region / City:
Australia
Topic:
Immunization, Respiratory Syncytial Virus (RSV), Vaccines
Document Type:
Submission
Organization:
SANOFI-AVENTIS AUSTRALIA PTY LTD
Author:
Not specified
Target Audience:
Healthcare professionals, policy makers, immunization program administrators
Period of validity:
From 2024
Approval Date:
24 November 2023
Date of Changes:
17 January 2025
Date of Submission:
7 March 2024
Note:
Contextual Description
Year:
2023
Region / city:
Australia
Topic:
Vedolizumab submission for chronic pouchitis treatment
Document type:
Submission for listing of medicinal product
Agency:
Therapeutic Goods Administration (TGA)
Author:
Takeda Pharmaceuticals Australia Pty. Ltd.
Target audience:
Healthcare professionals, regulatory authorities
Effective period:
From 29 June 2023
Approval date:
29 June 2023
Modification date:
N/A
Year:
2025
Region / city:
N/A
Topic:
Intramuscular injection techniques
Document type:
Tip sheet
Organization / institution:
ClinicalKey for Nursing
Author:
Perry, A. G., LaPlante, N., Ostendorf, W. R., & Potter, P. A.
Target audience:
Healthcare professionals
Effective period:
N/A
Approval date:
N/A
Modification date:
N/A
Note:
Year
Theme:
Rheumatology, Methotrexate Therapy, Drug Interaction
Document Type:
Medical Guidelines
Target Audience:
Healthcare Professionals, Specialists
Year:
2020
Region / City:
Australia
Topic:
Pharmaceutical Benefits Scheme (PBS) listing
Document Type:
Committee Submission
Agency:
PBAC (Pharmaceutical Benefits Advisory Committee)
Author:
Committee Secretariat
Target Audience:
Healthcare professionals, PBAC members
Period of Effect:
From May 13, 2020
Approval Date:
May 13, 2020
Modification Date:
Not specified
Year:
2021
Region / City:
Australia
Topic:
Pharmaceutical Submission
Document Type:
Regulatory Submission
Agency / Institution:
PBAC
Author:
CELLTRION HEALTHCARE AUSTRALIA PTY LTD
Target Audience:
Healthcare professionals, regulatory authorities
Effective Period:
2021 and ongoing
Approval Date:
25 August 2021
Date of Changes:
March 2022
Year:
2022
Region / City:
Australia
Subject:
Pharmacology, Pharmaceutical Benefits Scheme (PBS)
Document Type:
Submission
Organization / Institution:
Sanofi-Aventis Australia Pty Ltd
Author:
Not specified
Target Audience:
Medical practitioners, healthcare professionals
Period of validity:
Not specified
Approval Date:
3 June 2022
Date of Changes:
Not specified
Contextual Description:
A regulatory submission detailing the request for listing of dupilumab in new forms for treating severe atopic dermatitis and uncontrolled severe asthma in pediatric patients under the PBS.
Year:
2017
Region / City:
Australia
Subject:
Medical treatment, pharmaceutical submission
Document Type:
Submission for Pharmaceutical Benefits Scheme (PBS) consideration
Organization:
Therapeutic Goods Administration (TGA), Pharmaceutical Benefits Advisory Committee (PBAC)
Author:
AbbVie Pty Ltd.
Target Audience:
Medical professionals, regulatory authorities
Effective Period:
2017–2024
Approval Date:
October 26, 2016
Amendment Date:
Not specified
Year:
2023
Region / City:
Australia
Topic:
Oncology, Urothelial carcinoma, Immunotherapy
Document type:
Medical submission
Organization / Institution:
Bristol-Myers Squibb Australia Pty Ltd
Author:
Unknown
Target audience:
Medical practitioners, healthcare professionals
Period of validity:
Ongoing
Approval date:
2023
Date of amendments:
N/A
Source:
TGA/PBAC Parallel Process
Indication:
First-line treatment for unresectable or metastatic urothelial carcinoma
Treatment phase:
Initial and Continuing treatment
Condition:
Unresectable or metastatic urothelial carcinoma
Treatment criteria:
Patient must meet specific clinical and therapeutic criteria
Year:
2020
Region / City:
Australia
Topic:
Medical Treatment, Pharmaceutical
Document Type:
Submission
Organ / Institution:
Novartis Pharmaceuticals Australia Pty Limited
Author:
Not specified
Target Audience:
Healthcare professionals, policymakers
Period of Validity:
Not specified
Approval Date:
Not specified
Date of Changes:
Not specified
Year:
2025
Region / City:
UK
Topic:
Healthcare, Medication Guidelines
Document Type:
Medical Protocol
Organisation:
National Ambulance Service Medical Directors (NASMeD)
Author:
Dr. Elizabeth Miller, Dr. Dave Macklin, Mr. Andy Curran, Rosie England, Cathryn James, Dan Haworth, Tracy Rogers, Jo Jenkins, Rosie Furner
Target Audience:
Registered healthcare professionals, Paramedics, Nurses, Midwives
Effective Date:
May 2023
Review Date:
October 2025
Expiry Date:
April 2026
Approval Date:
May 2025
Change History:
Includes updates to drug administration protocols and clinical guidelines
Note:
Version Number 2.3
Year:
2025
Region / City:
United Kingdom
Theme:
Sexual and Reproductive Health
Document Type:
Patient Group Direction (PGD)
Organisation:
Faculty of Sexual and Reproductive Health (FSRH)
Author:
Dr. Cindy Farmer, Michelle Jenkins, Elaine Scott, Kalpesh Thakrar, Sim Sesane, Tanya Lane, Kate Devonport, Chetna Parmar, Carmel Lloyd, Clare Livingstone, Portia Jackson, Kirsty Armstrong, Dipti Patel, Emma Anderson, Alison Crompton, Lisa Knight, Bola Sotubo, Tracy Rogers, Sandra Wolper, Jo Jenkins, Rosie Furner
Target Audience:
Registered healthcare professionals authorised to practice under this PGD
Period of Effect:
May 2023 - April 2026
Approval Date:
December 2022
Review Date:
October 2025
Expiry Date:
April 2026
Year:
2027
Region / city:
United States
Topic:
Medicare Drug Price Negotiation Program
Document type:
Supporting Statement
Organ / institution:
Centers for Medicare & Medicaid Services (CMS)
Author:
Centers for Medicare & Medicaid Services (CMS)
Target audience:
Pharmaceutical industry, healthcare professionals, policymakers
Period of validity:
2026-2028
Approval date:
Not specified
Modification date:
Not specified
Year:
2027
Region / City:
United States
Topic:
Healthcare Technology, Medical Devices
Document Type:
Tracking Form
Agency / Organization:
Centers for Medicare & Medicaid Services
Author:
Unknown
Target Audience:
Healthcare Providers, Medical Device Manufacturers
Effective Period:
Fiscal Year 2027
Approval Date:
Unknown
Date of Changes:
Unknown