World Conference Calendar

33818 Conferences

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The Europe Meets Russia Conference

The Europe Meets Russia Conference

Location: , Germany
Category: Education
Start Date: 04-22-2027
The Europe Meets Russia Conference: A Forum for Young Leaders “Strengthening the Political & Economic Relations: Building Dialogue through Diplomacy between Cultures” (Berlin, April 22nd – 26th, 2013) Seminar Agenda The EMR Forum is a network of young professionals & students from across the world, who have an interest in the European-Russian relationship. The program has been developed in recognition of the importance of the relationship between Russia, Europe, and the global political system. The ultimate goal of the forum is to educate, enhance and sustain the Russian-European relationship by empowering the next generation of young leaders from Europe and…
Fourth International conference on Education and Distance Learning

Fourth International conference on Education and Distance Learning

Location: , Sri Lanka
Category: Education
Start Date: 04-27-2019
As a scientific research conference organizers, The Global Academic Research Institute proudly organized Fourth International conference on Education and Distance Learning (04th ICEDL 2018) under the theme of “Flexible Education For All” With the successful completion of three conferences in 2015, 2016 and 2017 we would like to invite you to submit abstract papers for the for 04th International Conference on Education & Distance Learning on 27th April, 2018 with addressing the conference theme and the conference tracks. We welcome proposals for papers and invitations for abstract submissions are now open for both Oral and Poster presentations covering current research…
Third International conference on Digital Marketing

Third International conference on Digital Marketing

Location: , Sri Lanka
Category: Education
Start Date: 06-22-2018
As a scientific research conference organizers, The Global Academic Research Institute proudly organized Third International conference on Digital Marketing (ICDM 2018) under the theme of “Sustainable Communication for Local to Global” The term "Digital Marketing" is always distinguished to different philosophy, and the modern discipline has a clear set of antecedents including Online Marketing, Search Engine Marketing, Mobile Marketing, SEO and other fields concerned with normative determinations of what ought to be and with deducing the characteristics and functions of the ideal state. International Conference on Digital Marketing 2018 provides great platform to all academics, leading researchers, professionals to share…
Third International conference on Contemporary Issues in Marketing

Third International conference on Contemporary Issues in Marketing

Location: , Sri Lanka
Category: Education
Start Date: 06-22-2018
As a scientific research conference organizers, The Global Academic Research Institute proudly organized Third International conference on Contemporary Issues in Marketing (ICCIM 2018) under the theme of “contemporary issues in Marketing – theory and practice” Marketing has become a global language of the new millennia. However, with an increase in consumer power, strict legislation, and competition the job of marketers has become more complex and much like a boundary-spanner. The Organizing Committee welcomes you all to attend and present your ideas to counter these challenges facing marketers of today at the International Conference on Contemporary Issues in Marketing to be…
International conference on Agribusiness Marketing

International conference on Agribusiness Marketing

Location: , Sri Lanka
Category: Education
Start Date: 05-18-2018
As a scientific research conference organizers, The Global Academic Research Institute proudly organized International conference on Agribusiness Marketing (ICABM 2018) under the theme of "Sustainable Agriculture Business for the Future" The term "Agribusiness Marketing" used in context of modern philosophy and discipline has a clear set of antecedents that include Agricultural Products, Agricultural Cooperatives, and Agricultural & Food Marketing Management, Sustainable Agriculture, Organic Agriculture, Agricultural Marketing Strategies and every other Agribusiness Marketing field. The term covers any field concerned with normative determinations of what ought to be and deduction of characteristics and functions of the ideal operation state. International Conference…
Second International conference on Language and Literature

Second International conference on Language and Literature

Location: , Sri Lanka
Category: Education
Start Date: 04-27-2018
As a scientific research conference organizers, The Global Academic Research Institute proudly organized Second International conference on Language and Literature (02nd ICLLS 2018) under the theme of “Creative Communication in a Global Context” Language is a system of conventional spoken, manual, or written symbols by means of which human beings, as members of a social group and participants in its culture, express themselves. Literature is an imaginative or creative writing, especially of recognized artistic value: "Literature must be an analysis of experience and a synthesis of the findings into a unity. International Conference on Language and Literature Studies 2018 will…
NDAs and INDs for Orally-Administered Drug Products

NDAs and INDs for Orally-Administered Drug Products

Location: , United States
Category: Education
Start Date: 02-28-2018
Overview: This webinar will be helpful to applicants conducting BA/BE studies during the IND period, also FDA guidance recommendations on how to meet the BA and BE requirements in 21 CFR 320 as they apply to oral dosage forms. Why should you Attend: Understanding when Bioavailability and Bioequivalence studies should be done can help attendees avoid having to re-do clinical trials, help to determine dosage regimen that achieves target drug exposure. Areas Covered in the Session: Review definitions necessary for understanding bioavailability and bioequivalence Review of FDA guidance recommendations on how to meet the BA and BE requirements in 21…
How Ensuring Data Integrity in Method Validations

How Ensuring Data Integrity in Method Validations

Location: , United States
Category: Education
Start Date: 02-28-2018
Overview: The webinar will also illustrate the lifecycle management of analytical procedures and train attendees on documentation requirements to ensure Data Integrity. Why should you Attend: The guidance changes how FDA regulated methods will be developed, validated and used. Additionally, how to ensure Data Integrity will be discussed. The webinar will focus on detailing all key components of the guidance and analyze its validation parameters, tests, and acceptance criteria with respect to Data Integrity. Areas Covered in the Session: Scope and Content of the Guidance Performing Pre-Validation Studies Analytical Method Transfer Studies Data Integrity and Documentation Requirements Who Will Benefit:…
Underutilized and Underappreciated in Management Control

Underutilized and Underappreciated in Management Control

Location: , United States
Category: Education
Start Date: 02-21-2018
Overview: In the highly regulated medical device industry, management responsibility and management review are critical concepts in ensuring a suitable Quality Management System (QMS). Why should you Attend: Management with executive responsibility is responsible for establishing a quality policy and objectives and for demonstrating a commitment to quality. And management at all levels should be aware of and engaged in quality efforts and customer focus. Areas Covered in the Session: Park Doctrine Lessons Learned Effective Management Review How to prioritize, resource, and implement improvements Tools for monitoring and communicating risk and improvement over time How to identify residual risk Who…
Learn Some of the Acceptance Activities in FDA QSR

Learn Some of the Acceptance Activities in FDA QSR

Location: , United States
Category: Education
Start Date: 02-21-2018
Overview: This section plays a major role in both purchasing and in production. It is a major contributor to determine whether your supplier and manufacturing process are working effectively. Why should you Attend: As you ensure that your Quality Management System meets FDA's regulations, you need robust acceptance activities. A gap could result in a Warning Letter, but even worse, it could also create a recall. This presentation provides the implementation information as well as the audit strategy to help verify your processes. Who Will Benefit: Operations Managers Production Supervisors Purchasing Managers Quality Engineers Manufacturing Engineers Speaker Profile: Dan is…
How to Comply with both in the Same Organization

How to Comply with both in the Same Organization

Location: , United States
Category: Education
Start Date: 02-16-2018
Overview: This ISO 13485:2016 webinar is a standard for Quality Management Systems of medical device manufacturers and suppliers, and is used worldwide for developing and maintaining the system that caters to the needs of the market requirements for medical devices. Why should you Attend: For people in the medical devices industry which either develops or planning to market medical devices to USA and Europe and plan to implant a QMS that complies with both regulatory authorities and ask themselves how to do it correct and efficiently. Areas Covered in the Session: Introduction Brief review of regulations and standard: status and…
Final Rules of Unique Device Identification

Final Rules of Unique Device Identification

Location: , United States
Category: Education
Start Date: 02-14-2018
Overview: This webinar will address the four key steps to compliance by device manufacturers. Also covered will be the Final Rule's provisions to address existing FG inventory, not properly labeled. Why should you Attend: It will also review the implementation schedule which is required of medical device companies selling products in the U.S. This is a major change for medical device manufacturers, with far-reaching effects in regulatory compliance, as envisioned by the FDA. Areas Covered in the Session: Learn the basic requirements of UDI Labeling and its Database UDI / GUDID Implementation Schedules Required steps for UDI / GUDID compliance…
How to plan risk based approaches for clinical trials

How to plan risk based approaches for clinical trials

Location: , United States
Category: Education
Start Date: 02-12-2018
Overview: You will understand how to identify, evaluate and also how to implement specific risk based techniques for risk management used in clinical trials. Areas Covered in the Session: Have explained key risk based process/tools and techniques Review a risk based approach to protocol design Understand risk based approach to monitoring / data handling Review of risk based approaches to QC / QA (Auditing) Hear best practice of these new risk requirements Who Will Benefit: Clinical Development Managers and Personnel Clinical Research Associates Clinical Research Archiving and Document Management Personnel Quality Assurance Managers and Auditors Clinical Development Managers and Personnel…
Practices for Active Pharmaceutical Ingredients per ICH Q7

Practices for Active Pharmaceutical Ingredients per ICH Q7

Location: , United States
Category: Education
Start Date: 02-08-2018
Overview: The APIs covered in this guidance document include new chemical entities and APIs of biological origin and those created by biotech processes. Why should you Attend: This document was created to fulfil the need for specific guidance with regards to GMPs for APIs. Failure to meet these requirements is a significant source of observations during regulatory inspections by FDA or global regulators of manufacturers and/or of sponsors that use contract manufacturers and the contract manufacturers themselves. Areas Covered in the Session: Validation of Analytical Procedures, C of As, Stability Monitoring, Expiry dating Validation Policy, Documentation, Qualification, Process validation, Validation…
Why Capturing Justifications in Change Control

Why Capturing Justifications in Change Control

Location: , United States
Category: Education
Start Date: 02-07-2018
Overview: It is easy to document what process has been performed, what has been investigated or changed or why something is a risk, but the difficult part is knowing how to explain or justify why it should be done or why a product should be released or rejected as a result. Areas Covered in the Session: Determine alternatives or options to the proposed solution Analyze costs, benefits, impacts, and risks of the proposed solution Validate the solution, assess product impact to the market Who Will Benefit: Quality Assurance/Quality Control Directors, Managers,and Specialists Regulatory Affairs/Regulatory Compliance Directors, Managers,and Specialists Engineering/Development Directors,…
How to Accurate Adverse Event Reporting

How to Accurate Adverse Event Reporting

Location: , United States
Category: Education
Start Date: 02-06-2018
Overview: Learn why the single most important function of the Principal Investigator and the study conduct team is the awareness, assessment, and management of Adverse Events occurring during the conduct of clinical research with drugs or devices utilizing human subjects. Why should you Attend: With the increasing complexity of the Investigational Medicinal Products (IMP's), it behooves all who have any role in observing Study Participants to know the importance of accurately collecting all AE and SAE data. Areas Covered in the Session: How to know what an Adverse Event is and when to report it or them Knowing the AE…
How to Validate for Regulated Computer Systems

How to Validate for Regulated Computer Systems

Location: , United States
Category: Education
Start Date: 02-02-2018
Overview: You'll learn about the various computer system validation deliverables and how to document them through the entire process. You will learn about what must be done to ensure the system remains in a validated state. Why should you Attend: This webinar will help you understand in detail Computer System Validation (CSV) and how to apply the System Development Life Cycle (SDLC) Methodology when validating computer systems subject to FDA regulations. Areas Covered in the Session: Installation Qualification Operational Qualification Performance Qualification Policies and Procedures Training Organizational Change Management Who Will Benefit: Clinical Data Managers and Scientists Compliance Managers and…
Aware of the Similarities and Differences in the files

Aware of the Similarities and Differences in the files

Location: , United States
Category: Education
Start Date: 01-31-2018
Overview: It will also consider the European Union's MDD TF/DD requirements, and evaluate the documents' differing purposes / goals, as well as the two different device classification schemes. Why should you Attend: companies go global, they must meet different product design documentation. The cGMPs mandate Design Control and the Design History File (DHF). In order to sell globally, the EU's CE-marking documentation is a requirement - the Technical File or Design Dossier. Areas Covered in the Session: DHF "Typical" Contents and Deliverables The DMR and DHR / Lot / Batch Record TF / DD Required Contents Parallel Approaches to Documentation…
Which data and systems are subject to Part 11

Which data and systems are subject to Part 11

Location: , United States
Category: Education
Start Date: 01-16-2018
Overview: This webinar details the regulation and how it applies to computerized systems. Learn exactly what is needed to be compliant for all three primary areas: SOPs for the IT infrastructure, industry standards for software product features, and the 10-step risk-based validation approach. Areas Covered in the Session: Which data and systems are subject to Part 11 What Part 11 means to you, not just what it says in the regulation Avoid 483 and Warning Letters Explore the three primary areas of Part 11 compliance: SOPs, software product features, and validation documentation Ensure data integrity, security, and protect intellectual property…
The Value of a Human Factors Program

The Value of a Human Factors Program

Location: , United States
Category: Education
Start Date: 01-12-2018
Overview: This webinar will explain the implementation of ISO 62366 and the regulatory expectations discussed in the 2016 FDA Guidance for a compliant human factors/ usability program. Why should you Attend: This year FDA published their priority list for the completion of their Guidance documentation. This annual activity gives us inspection and enforcement insight into the priorities within the agency. Interoperability and Cybersecurity were in the top 3. The implementation of a robust HF program will include both of these disciplines. Following the implementation of the results of a Human Factors/ Usability study, a validation of the safety and effectiveness…

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