HYBRID EVENT
: You Can Participate In Person At
Florence, Italy
Or Virtually From Your Home Or Work
☰
Home
About
About Organization
Testimonial
Call For Paper
Abstract Submission
Registration
Registration
Refund Policy
Program
Tentative Program
Scientific Session
Technical Program Committee
Eligibility & Roles
Apply for Committee
Committee Members
Information
Venue
Guidelines
Important Dates
Past Speakers
Conference Flyer
Conference Speakers
Speaker Criteria
Submit Proposal
Past Speakers
Journal Publication
FAQ
Venue
Contact
ICPLDRPS · Registering as Listener
International Conference on Pharmaceutical Law, Drug Regulation, and Patient Safety
26–27 Dec 2026
Florence, Italy
Standard / Physical
Participation
Listener Registration
$
135
virtual · $175 in person
Registration Benefits:
Official invitation letter
Issued automatically after registration
Certificate & digital materials
Get certificate, slides and resource materials
Supporting global research
Connect with researchers across 30+ countries
Credit Card
Debit Card
Net Banking
Cash Card
Unified Payments
Select registration mode
Prices are shown before tax and bank charges — no surprises at checkout.
Standard / Physical
$175
On-site keynotes, talks, workshops, networking, conference kit and certificate.
Select
Virtual
$135
Live streaming access to all sessions, digital materials and certificate.
Select
All sessions
Networking
Certificate
Invitation letter
Conference kit
Your details
We only need what's required to register and email your confirmation. Everything else is optional.
Full name
*
Email address
*
Mobile number
*
City
*
State
*
Country
*
Select country
Zip / Postal code
Address
Coupon code
Have a code? Apply it here — the discount updates the total immediately.
Apply
1. Policy on Cancellations & Refunds :
A full refund is possible only if the cancellation request is submitted at least 70 days before the conference, with formal paperwork completed at least 60 days prior.
If cancellation occurs between 60 and 30 days before the event, partial refunds may be granted based on administrative costs incurred.
Cancellations made within 30 days of the event are non-refundable, though participants will receive a credit valid for one year.
Registrations made less than 30 days before the event are not eligible for refunds, but may be transferred to another ISIT conference.
Since this conference is hybrid format, the organizer reserves the right to conduct the event either in-person or virtually. Please note that no refunds will be issued due to changes in the event format.
Virtual registration fees are non-refundable. A credit will instead be issued for use at a future conference event.
2. Participation & Registration Requirements :
To attend an ISIT event, participants must complete the registration process within the stipulated time.
The event schedule, venue, and format are subject to changes at the discretion of the organizers, with prior notice sent via email.
ISIT is not liable for any financial losses resulting from changes in event details.
Fees paid for registration are strictly non-refundable.
If the primary author cannot participate, a co-author may attend instead, but refunds will not be granted for non-attendance.
3. Submission & Publication Norms :
Researchers submitting papers to ISIT must ensure their institution or supervisor is aware of their submission.
Each submission is subject to a rigorous peer review before being accepted for presentation.
Only papers linked to a completed registration will be included in conference proceedings.
The submitting author is considered the primary author; ISIT does not verify individual authorship claims.
If any concerns regarding authorship arise and are validated, the paper will be withdrawn without reconsideration.
Once a paper is removed, it cannot be reintroduced into any ISIT publication.
4. Travel & Accommodation Responsibilities :
Attendees are responsible for making their own travel and lodging arrangements.
ISIT does not provide logistical assistance for travel or accommodation.
The organization bears no responsibility for expenses incurred due to conference modifications or rescheduling.
5. Visa & Invitation Letter Policy :
Attendees are responsible for making their own travel and lodging arrangements.
ISIT does not provide logistical assistance for travel or accommodation.
The organization bears no responsibility for expenses incurred due to conference modifications or rescheduling.
ISIT does not engage directly with consulates or embassies on behalf of attendees.
Participants must handle their own visa applications and processes.
Important Information Regarding Invitation Letters:
The invitation letter is provided solely for conference attendance and does not serve as a document for immigration, employment, or residency purposes.
The letter assists in visa applications but does not guarantee visa approval.
ISIT holds no responsibility for visa denials or processing delays, and all related costs are borne by the applicant.
Any alterations or unauthorized use of the invitation letter will result in its invalidation and possible cancellation of conference participation.
Legal action may be pursued if the document is misused.
By accepting the invitation letter, attendees agree to comply with international travel regulations and ethical participation standards.
6. Registration Transfers :
Registrations may be transferred to another individual from the same institution if the original participant cannot attend.
Transfer requests must be made via email to
[email protected]
with necessary details and supporting documents.
Transfers must be requested at least 14 days before the event; otherwise, they will not be accommodated.
Transferred registrations are not eligible for refunds.
7. General Considerations :
Any modifications or cancellations must be communicated in writing to
[email protected]
.
Registration confirms acknowledgment and acceptance of these policies.
ISIT does not initiate automatic transactions; all payments are voluntarily completed by registrants.
Once registered, participants must submit a conference registration form within three days for confirmation.
Travel plans should only be finalized after receiving the official conference itinerary, which will be shared 15 days before the event.
8. Conference Programme and Participation Policy :
Presentations from different but relevant academic areas may be combined by the Organiser within an interdisciplinary or multidisciplinary programme to encourage cross-disciplinary understanding, interaction, and future research partnerships.
I agree to the
Terms & Conditions
and
Refund & Cancellation Policy
.
Continue to payment →
Payments encrypted & processed securely. Refundable up to 14 days before the event.
What you'll hear about
Session tracks covered across the event.
View all 11 tracks →
01
Pharmaceutical Law Fundamentals
This track will explore the foundational principles of pharmaceutical law, including the legal frameworks governing drug development and approval processes. Participants will gain insights into the interplay between law and the pharmaceutical industry.
02
Regulatory Oversight in Drug Approval
This session will focus on the role of regulatory agencies in the drug approval process, examining the standards and guidelines that govern pharmaceutical products. Discussions will include the impact of regulatory decisions on public health and safety.
03
Ethical Considerations in Clinical Trials
This track will address the ethical dilemmas faced during clinical trials, including informed consent and participant safety. Experts will discuss the balance between scientific advancement and ethical responsibility.
04
Medication Compliance and Patient Safety
This session will investigate the legal implications of medication compliance and its impact on patient safety. Participants will explore strategies to enhance adherence to prescribed therapies while minimizing legal risks.
05
Pharmacovigilance and Risk Management
This track will delve into the legal frameworks surrounding pharmacovigilance and the importance of monitoring drug safety post-approval. Discussions will highlight the responsibilities of pharmaceutical companies in managing risks associated with their products.
06
Prescription Law and Patient Rights
This session will examine the legal aspects of prescription law, focusing on patient rights and the responsibilities of healthcare providers. Participants will analyze case studies that highlight the intersection of law and patient care.
07
Drug Liability and Legal Accountability
This track will explore the legal liabilities associated with pharmaceutical products, including issues of negligence and product liability. Legal experts will discuss landmark cases and their implications for the industry.
08
Health Policy and Pharmaceutical Governance
This session will focus on the intersection of health policy and pharmaceutical governance, examining how laws shape drug access and affordability. Participants will engage in discussions about policy reforms and their potential impact on public health.
09
FDA Compliance and Regulatory Challenges
This track will address the complexities of FDA compliance, including the challenges faced by pharmaceutical companies in meeting regulatory requirements. Experts will provide insights into best practices for navigating the regulatory landscape.
10
Safety Standards and Quality Assurance
This session will explore the legal standards for safety and quality assurance in pharmaceutical manufacturing. Participants will discuss the implications of non-compliance and the role of law in ensuring product safety.
11
Emerging Trends in Health Care Law
This track will examine the latest developments in health care law as they pertain to the pharmaceutical industry. Discussions will include the impact of technological advancements and evolving legal frameworks on drug regulation.