Request for proposals
|RFP ID||Product||Issues date||Title||Close date|
|EXP101||EXPAREL||May 14, 2020||EXPAREL use in hip fracture repair||Open|
|IOV102||ioverao||May 14, 2020||ioverao use in chronic foot pain||Open|
|IOV103||ioverao||May 14, 2020||ioverao use in shoulder disorders||Open|
|IOV104||ioverao||May 14, 2020||ioverao use in muscle spasticity||Open|
|IOV105||ioverao||June 1, 2020||ioverao use in rib fracture||Open|
|IOV106||ioverao||June 1, 2020||ioverao use in pectus excavatum correction||Open|
|IOV107||ioverao||June 1, 2020||ioverao use in postherpetic neuralgia||Open|
Introduction to Pacira
Pacira BioSciences, Inc. is committed to supporting independent research initiatives that foster the advancement of scientific and clinical information and improve patient care. To that end, Pacira extends a new grant opportunity by way of a request for proposal (RFP) focused on research trials that seek to result in optimized patient care. These research trials will provide valued information on the efficacy of the company’s marketed products.
All proposals are reviewed for scientific merit, innovation, clinical impact on patients, and compliance with Pacira policy and requirements. If you are interested in applying for support of a research proposal, please review the submission process and apply online by clicking here. Pacira will review and consider all relevant research proposals but is not obligated to provide support for any research proposals received.
While the Pacira Grant Review Committee (PGRC) reviews all research proposals, the principal investigator (and ultimately the grantee) is responsible for the design, implementation, and conduct of the independent initiative supported by the grant. Pacira will not be involved in the conduct or monitoring of the proposed trial, including drafting the research study protocol.
Request for proposals
A RFP is a company announcement that publishes and details a planned project and invites researchers to submit a proposal.
The principal investigator or institution designs and implements the research study and acts as the study sponsor. The study sponsor is the individual (or entity) responsible for complying with all applicable regulatory requirements, guidance, and laws related to the research study. This also includes registering the study with appropriate governmental agencies and websites (eg, https://clinicaltrials.gov/) and reporting safety data to all relevant regulatory authorities.
The research must aim to contribute to the greater scientific community, and the budget must be reasonable and appropriate for the proposed research study. In considering RFPs, Pacira will consider, among other factors, the expertise of the principal investigator and any co-investigators, including their experience in the relevant therapeutic area, demonstrated ability to conduct clinical trials successfully, and available resources.
The sponsor-investigator (ie, principal investigator) will have full and final discretion and responsibility for all aspects of the study design, implementation, data analysis, and data dissemination, including compliance with all laws and regulations applicable to research sponsors.
Please note that study approval and ultimately funding is not contingent upon the use, purchase, or recommendation of Pacira products.
The RFP process
Pacira maintains a stepwise process for review of RFPs. In brief, after registering on the online grant portal, the principal investigator submits a brief concept proposal and if accepted after a review by the PGRC, will be invited to submit a full proposal. Details on brief and full proposal contents are below.
Brief concept proposal:
A brief concept proposal must contain an adequate amount of information for the PGRC to determine interest in requesting a full study proposal. When submitting a brief concept proposal, the following information will be requested (if applicable):
- Principal investigator contact information
- Brief background for the study
- Method of administration of the marketed product
- Primary study objectives/endpoints
- Estimated study timelines
- Estimated total study budget
- Estimated study drug or device(s)
- Preliminary grant request: funding, drug, device, or a combination thereof
- Experience as sponsor-investigator
- Letter of intent on the requesting institution’s letterhead
- Curriculum vitae from the principal investigator dated within the last calendar year
The PGRC will review all concept proposals for scientific merit, innovation, clinical importance/potential impact on patients, and compliance with company policy and requirements. The PGRC will extend contingent approval to individual applicants to proceed to the second step of the process, which is the submission of a full study proposal. Applicants will be notified of the PGRC’s decision via email, and the status will also be available on the portal. Please note that an invitation to submit a full study proposal does not guarantee the approval of funding.
Full study proposal:
A full study proposal submission must contain enough detail about the research study to enable the PGRC to make an evaluation on support. When submitting a full study proposal, the following information will be requested (if applicable):
- Principal investigator contact information
- Study type: non-clinical or clinical
- Objectives: primary and secondary
- Key inclusion and exclusion criteria
- Study design
- Efficacy variables/measures
- Safety variables/measures
- Adverse event/Serious adverse event reporting
- Decision points/statistical methods/interim analysis
- Study product regimens
- Ethical rationale for the study
- Study deliverables
- Value of the study
- Applicable scientific references
- Publication plan
- Research Setting: single-site or multi-site
- Detailed budget
- Grant request: funding, product, or a combination thereof
Pacira reserves the right to reconsider its support if the research objectives outlined in the final protocol are materially different from the approved full study proposal. Pacira will not compensate for any work performed before the execution of a final contract or for impermissible costs, which include:
- Construction funds to build new facilities
- General education and training activities
- Hiring of staff that are not dedicated to the proposed research study
- Study to involve new investigational products or devices
- Studies that are designed to generate business for Pacira
- Purchase of capital equipment unrelated to the study or that would generate revenue
- Requests for support for ongoing or new research without an associated research study protocol
- Start-up funds to establish new clinical or research programs or to expand existing programs
- Support for ongoing clinical programs that are part of an organization's routine operations
Pacira requires the grant recipient(s) to comply with all applicable laws, rules, regulations and industry codes related to clinical and/or non-clinical research, including registration of protocols and posting of results such as on FDA's ClinicalTrials.gov database or another trial registry website as well as Adverse Event reporting.
Please note, all IRB approvals must be received within four months of when Pacira executes the Agreement. If this deadline is not met, Pacira reserves the right to rescind approval of the grant support.
Applicants whose proposal has been approved will be sent an Agreement that will set forth the obligations with respect to the study. Applicants will have four weeks from the date the Agreement is sent/emailed/uploaded to review, sign, and return the Agreement. If the Independent Research Agreement is not returned within four weeks, the contingent approval may be withdrawn.
Monthly study status update
Pacira requires at least one study status update per month. Updates should include current enrollment figures (if applicable) and the projected completion date (if different from the previously reported date). Pacira also requires disclosure of any protocol changes made since the commencement of the research.
The principal investigator (ie, sponsor-investigator) is required to provide Pacira with a written manuscript quality report of the final study results. Upon study closure, the investigator is required to provide a detailed budget reconciliation demonstrating that grant funds and/or product were used solely to conduct the study, all safety reporting obligations were met, and unused study drugs/products were destroyed or returned in accordance with the organization’s policies.
Pacira supports the exercise of academic freedom and encourages the publication of study results, whether favorable or not to Pacira and its products. Furthermore, Pacira maintains the right to review each publication and/or presentation (including, but not limited to, full manuscripts, abstracts, poster presentations, and oral presentations) of results of the research prior to its submission to anyone not affiliated with Pacira or the principal investigator.
The principal investigator will comply with recognized ethical standards concerning publications, authorship and disclosure of funding, including without limitation the Uniform Requirements for Manuscripts Submitted to Biomedical Journals, www.icmje.org, established by the International Committee of Medical Journal Editors.