<?xml version="1.0" encoding="UTF-8"?><rss version="2.0"
	xmlns:content="http://purl.org/rss/1.0/modules/content/"
	xmlns:wfw="http://wellformedweb.org/CommentAPI/"
	xmlns:dc="http://purl.org/dc/elements/1.1/"
	xmlns:atom="http://www.w3.org/2005/Atom"
	xmlns:sy="http://purl.org/rss/1.0/modules/syndication/"
	xmlns:slash="http://purl.org/rss/1.0/modules/slash/"
	>

<channel>
	<title>certificate course in pharmacovigilance &#8211; Global Pharma</title>
	<atom:link href="https://globalpharmaacademy.com/product-tag/certificate-course-in-pharmacovigilance/feed/" rel="self" type="application/rss+xml" />
	<link>https://globalpharmaacademy.com</link>
	<description>Academy</description>
	<lastBuildDate>Sun, 14 Jan 2024 12:08:10 +0000</lastBuildDate>
	<language>en-US</language>
	<sy:updatePeriod>
	hourly	</sy:updatePeriod>
	<sy:updateFrequency>
	1	</sy:updateFrequency>
	<generator>https://wordpress.org/?v=6.9.4</generator>

<image>
	<url>https://globalpharmaacademy.com/wp-content/uploads/2020/12/cropped-LOGO-GPA-JPG-32x32.jpg</url>
	<title>certificate course in pharmacovigilance &#8211; Global Pharma</title>
	<link>https://globalpharmaacademy.com</link>
	<width>32</width>
	<height>32</height>
</image> 
	<item>
		<title>Online course in Pharmacovigilance</title>
		<link>https://globalpharmaacademy.com/product/online-course-in-pharmacovigilance/</link>
					<comments>https://globalpharmaacademy.com/product/online-course-in-pharmacovigilance/#respond</comments>
		
		<dc:creator><![CDATA[Admin]]></dc:creator>
		<pubDate>Sun, 14 Jan 2024 12:08:10 +0000</pubDate>
				<guid isPermaLink="false">https://globalpharmaacademy.com/?post_type=product&#038;p=2887</guid>

					<description><![CDATA[Syllabus covered
1) Overview Clinical research and History and development of PV
2) Basics of Bioequivalence, Bioavailability, Pharmacodynamics and pharmacokinetics.
3) Adverse Drug Reactions, Key Terminologies in PV, Methodologies in Pharmacovigilance
4) Clinical trials-Types, Phases
5) ICSR management and case studies
6) MedDRA coding
7) Seriousness and causality assessment
8) Narrative writing
9) Safety database overview- example- Argus, Aware, Aris g etc.
10) Special scenario in PV
11) Signal detection and management
12) Overview of Periodic Safety Update Reports (PSURs), Aggregate reporting, medical writing, Importance of local literature search
13) MICC (Medical information contact center) overview
14) Pharmacovigilance System Master File (PSMF), Risk Management Planning (RMP), Reference Safety Information (RSI)
15) PV inspection and Audits
16) Contract research organization (CRO)
17) Pharmacovigilance Regulations in Various Countries

Along with this we provide skill development classes which covers
1)zresume preparation
2)HR question
3) individual mock interview
4)Job searching skill
5)presentation skill (PPT presentation)
6)HR communication skill
7)effective email writing skill

Benefits of course
1) Certification from ISO certified organization
2) Expert guide having more than 10+ year of experience in core pharmacovigilance domain
3) Live lectures with recording
4) 100% placement assistance
5) study material provided]]></description>
										<content:encoded><![CDATA[<p>Syllabus covered<br />
1) Overview Clinical research and History and development of PV<br />
2) Basics of Bioequivalence, Bioavailability, Pharmacodynamics and pharmacokinetics.<br />
3) Adverse Drug Reactions, Key Terminologies in PV, Methodologies in Pharmacovigilance<br />
4) Clinical trials-Types, Phases<br />
5) ICSR management and case studies<br />
6) MedDRA coding<br />
7) Seriousness and causality assessment<br />
8) Narrative writing<br />
9) Safety database overview- example- Argus, Aware, Aris g etc.<br />
10) Special scenario in PV<br />
11) Signal detection and management<br />
12) Overview of Periodic Safety Update Reports (PSURs), Aggregate reporting, medical writing, Importance of local literature search<br />
13) MICC (Medical information contact center) overview<br />
14) Pharmacovigilance System Master File (PSMF), Risk Management Planning (RMP), Reference Safety Information (RSI)<br />
15) PV inspection and Audits<br />
16) Contract research organization (CRO)<br />
17) Pharmacovigilance Regulations in Various Countries</p>
<p>Along with this we provide skill development classes which covers<br />
1)zresume preparation<br />
2)HR question<br />
3) individual mock interview<br />
4)Job searching skill<br />
5)presentation skill (PPT presentation)<br />
6)HR communication skill<br />
7)effective email writing skill</p>
<p>Benefits of course<br />
1) Certification from ISO certified organization<br />
2) Expert guide having more than 10+ year of experience in core pharmacovigilance domain<br />
3) Live lectures with recording<br />
4) 100% placement assistance<br />
5) study material provided</p>
<p><span id="more-2887"></span></p>
]]></content:encoded>
					
					<wfw:commentRss>https://globalpharmaacademy.com/product/online-course-in-pharmacovigilance/feed/</wfw:commentRss>
			<slash:comments>0</slash:comments>
		
		
			</item>
	</channel>
</rss>
