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International Conference on Pharmaceutical Engineering and Life Sciences (ICPELS-26)

20th - 21st August 2026 Moscow, Russia
Hybrid Access Invitation Support

Join researchers, academicians, professionals, and industry experts to exchange ideas, strengthen academic collaboration, and explore research-driven practices across diverse disciplines.

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Professional Academic Experience

Participate in structured academic sessions, expert discussions, and professional knowledge-sharing opportunities.

Official Invitation Letter Available

Registered listeners can request an official invitation letter after successful registration confirmation.

Benefits of Registering as Listener
Access to Conference Sessions

Attend keynote, plenary and technical sessions across relevant academic tracks.

Academic Networking

Connect with researchers, professionals, academicians and industry specialists.

Certificate of Participation

Receive an official participation certificate after successful attendance.

Invitation Letter Support

Request official invitation letter support after confirmed registration.

Conference Materials

Access available session resources, proceedings and digital materials.

Professional Insights

Gain practical and research-oriented insights from expert discussions.

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4 Terms & Condition
Refund, Cancellation, Postponement, Travel and Transfer of Registration:
Refund Policy:

If the registrant is unable to attend and is not in a position to transfer his/her participation to another person or event, then the following refund arrangements apply: Keeping given advance payments towards Venue, Printing, Shipping, Hotels, and other overheads, we had to keep the Refund Policy as the following slabs:

1. Cancellations made before 60 days of the conference are eligible for a full refund, subject to a $100 cancellation charge.
2. Cancellations made within 60-30 days of the conference are eligible for a 50% payment refund.
3. Cancellations made within 30 days of the conference are not eligible for a refund.
4. Virtual Participation registrations are non-refundable.

(a) The above refund policies are applicable only if the registrant has not received the official invitation letter for participation in the event, If the client receives the conference invitation letter but cannot attend the conference, no refund will be provided.

(b) If the client cannot attend the conference for any personal reasons, the registration fee is not refundable. However, the fee will be considered as a credit to participate in any of our international conferences within one year from the date of registration.

(c) In the event of a visa denial, travel reasons, or natural calamities preventing attendance, the registration fee will not be refunded. However, the fee will be considered as a credit to participate in any of our international conferences within one year from the date of registration.

(d) Since this conference is hybrid, the organizer reserves the right to conduct it in any format, physical or virtual. Refunds will not be provided for format changes.

(e) For participants who register close to the conference date or after the standard registration deadline, The registration will be considered for virtual participation only, as the conference is in hybrid mode. However, you will be eligible to attend one more international conference based on your registration category.

Cancellation Policy:

If the organizer cancels this event for any reason, you will receive a credit for 100% of the registration fee paid. You may use this credit for another event which must occur within one year from the date of cancellation.

Postponement of Event:

If the organizer postpones an event for any reason and you are unable or unwilling to attend on rescheduled dates, you will receive a credit for 100% of the registration fee paid. You may use this credit for another event which must occur within one year from the date of postponement.

Travel and Accommodation Responsibilities:

a) The responsibility for making and managing travel arrangements, including flights, transportation, and accommodation, lies solely with the individual participant.

b) In the event of any changes to the conference format, cancellation, or venue adjustments, the organizers cannot assume responsibility for any costs incurred by participants for travel or accommodation.

Transfer of registration:

All fully paid registrations are transferable to other persons from the same organization if the registered person is unable to attend the event. Transfers must be made by the registered person in writing to event@after.org.in. Details must include the full name of the replacement person, their title, contact phone number, and email address. All other registration details will be assigned to the new person unless otherwise specified. Registration can be transferred from one conference to another conference of the same organizer if the registrant is unable to attend one of the conferences

However, Registration cannot be transferred if it is intimated within 14 days of the respective conference. The transferred registrations will not be eligible for Refund.

Visa Information:

The organizer will not directly contact embassies and consulates on behalf of visa applicants. All delegates or invitees should take responsibility for their visa and travel arrangements. Important note for failed visa applications: Visa issues cannot come under the consideration of the cancellation policy of the organizer, including the inability to obtain a visa.

N.B:

All cancellations or modifications of registration must be made in writing to event@after.org.in

I agree and accept the Terms and Conditions of the website www.after.org.in

Conference Session Tracks

Aligned with United Nations Sustainable Development Goals

Our conference tracks support global knowledge exchange, innovation, and sustainable development priorities across diverse disciplines.

SDG 3 SDG 4 SDG 9
01 Advancements in Drug Formulation Techniques
This track will explore innovative methodologies in drug formulation, focusing on enhancing bioavailability and therapeutic efficacy. Participants will discuss recent developments in excipient technology and formulation strategies for complex drug delivery systems.
02 Process Optimization in Pharmaceutical Manufacturing
This session will address the latest strategies in process optimization to improve efficiency and reduce costs in pharmaceutical manufacturing. Topics will include the application of lean manufacturing principles and advanced process control techniques.
03 Biopharmaceuticals: Challenges and Innovations
This track will delve into the unique challenges associated with the development and production of biopharmaceuticals. Discussions will focus on innovative solutions for scaling up production and ensuring product quality.
04 Molecular Biology Applications in Drug Development
This session will highlight the role of molecular biology techniques in the drug development process. Participants will examine case studies demonstrating the impact of genetic engineering and biomolecular analysis on therapeutic advancements.
05 Innovations in Drug Delivery Systems
This track will focus on cutting-edge technologies in drug delivery systems, including nanoparticles, liposomes, and smart drug delivery mechanisms. The session aims to foster discussions on improving targeted delivery and patient compliance.
06 System Modeling in Biomedical Engineering
This session will explore the application of system modeling techniques in biomedical engineering to enhance the understanding of complex biological systems. Participants will discuss computational models that aid in predicting drug behavior and patient outcomes.
07 Bioprocessing Techniques for Enhanced Production
This track will cover advanced bioprocessing techniques that optimize the production of biopharmaceuticals and biologics. Emphasis will be placed on fermentation technology, cell culture optimization, and downstream processing.
08 Regulatory Compliance in Pharmaceutical Engineering
This session will address the critical aspects of regulatory compliance in pharmaceutical engineering. Discussions will focus on navigating the regulatory landscape to ensure product safety and efficacy throughout the development process.
09 Quality Control and Assurance in Life Sciences
This track will examine the latest methodologies in quality control and assurance within the life sciences sector. Participants will discuss best practices for maintaining high standards in pharmaceutical production and testing.
10 Therapeutic Development and Healthcare Innovation
This session will explore the intersection of therapeutic development and healthcare innovation, focusing on novel therapeutic approaches and technologies. Participants will share insights on how innovation can drive improvements in patient care.
11 Bioengineering Solutions for Modern Healthcare
This track will highlight the role of bioengineering in addressing contemporary healthcare challenges. Discussions will include the development of bioengineered products and systems that enhance patient outcomes and healthcare delivery.