Csaba Hetenyi

Csaba Hetenyi

Research Associate Professor
Hungarian Academy of Sciences, Hungary
LINKS
http://xray.bmc.uu.se/~csaba/hetenyi_short_bio.pdf
http://scholar.google.hu/citations?user=b1FesyEAAAAJ&hl
E-mail megerősítve itt: caesar.elte.hu - Kezdőlap
http://www.researcherid.com/rid/G-5249-2010
https://hu.linkedin.com/pub/csaba-hetényi/17/9b4/25b
http://loop.frontiersin.org/people/58310/bio



Summary
Dr. Csaba Hetenyi is a Qualified Chemist, and a PhD in Pharmacy. He has co-authored research articles in prestigious journals J Am Chem Soc, PNAS, EMBO Reports, Bioinformatics, and is also a co-inventor of US patents.
Dr. Hetenyi has received more than one thousand citations for his research results and his works were favorably evaluated by several review articles and research papers.
In 2011, Dr. Hetenyi won a Talentum Academy Award for his research achievements. His primary interest is focused on chemical biophysics, computational and medicinal chemistry, structural bioinformatics, molecular pathomechanisms of diseases.
He has also contributed to publications in the fields of chromatography and capillary electrophoresis.
Dr. Hetenyi works in Hungary with three PhD students.
Qualifications
PhD, Pharmacy (summa cum laude), Faculty of Pharmacy, University of Szeged, Hungary, 2002.
MSc, Qualified Chemist (with distinction), Faculty of Science, University of Szeged, Hungary, 1999.
Research interests General: Chemical biophysics Computational and medicinal chemistry Structural bioinformatics Molecular pathomechanism of diseases Chromatography and capillary electrophoresis (formerly) Specific: Molecular mechanics & dynamics, docking Calculation of macromolecular structures and ligand-target interactions Thermodynamics of molecular complexes Quantitative structure-activity relationships Computer-aided drug design Application of quantum chemical methods

Experience

Sr. Research Fellow

Hungarian Academy of Sciences

June 2012 – Present (3 years 5 months)Budapest

MTA-ELTE Molecular Biophysics Research Group

Sr. Research Fellow

Eötvös University

December 2009 – May 2012 (2 years 6 months)

Research and teaching.

Visiting Scientist

Uppsala University

July 2009 – December 2009 (6 months)Uppsala, Sweden

Research

Sr. Researcher

University of Tartu

2006 – 2008 (2 years)

Teaching, research.

Molecular Biophysics Research Group, Hungarian Academy of Sciences

c/o Dept. of Biochemistry, Eotvos University

Pazmany stny. 1/C, 1117 Budapest, Hungary

Room 7.427

Phone 1: +3614116500/8697

Phone 2: +3613812171

Fax: +3613812172

E-mails:

Education

University of Szeged

PhD, Pharmacy

1999 – 2002

University of Szeged

MSc, Chemistry

1994 – 1999

József Attila Grammar School, Székesfehérvár

1989 – 1994

 

Dr. Csaba Hetényi is a Research Associate Professor at the Molecular Biophysics Research Group of the Hungarian Academy of Sciences. He is a qualified chemist and has a PhD in Pharmacy. He has co-authored research articles in prestigious journals such as J Am Chem Soc, EMBO Reports, FASEB J, etc. and has already received more than one thousand citations for his research results. His works were favorably evaluated by several review articles. He is also co-inventor in three US patents. In 2011, Dr. Hetényi received the prestigious Talentum Academy Award of the Central-European Talent Search Foundation. Dr. Hetényi’s primary research interests focus on chemical biophysics, computational and medicinal chemistry, structural bioinformatics, molecular pathomechanisms of diseases, and he has also published works in the fields of chromatography and capillary electrophoresis.
Chemical biophysics, computational and medicinal chemistry, structural bioinformatics 

SELECTED PUBLICATIONS

Jeszenoi N, Horvath I, Balint M, van der Spoel D, Hetenyi C* (2015) Mobility-based prediction of hydration structures of protein surfaces. Bioinformatics, 31, 1959-65 Program MobyWat is available here   Garcia-Sosa AT, Maran U, Hetenyi C* (2012) Molecular property filters describing pharmacokinetics and drug binding. Curr Med Chem 19, 1646-62   Hetenyi C*, van der Spoel D (2011) Toward prediction of functional protein pockets using blind docking and pocket search algorithms. Protein Sci 20, 880-93   Takacs B, O'Neall-Hennessey E, Hetenyi C, Kardos J, Szent-Gyorgyi AG, Kovacs M (2011) Myosin cleft closure determines the energetics of the actomyosin interaction. FASEB J 25, 111-21   Org T, Chignola F, Hetenyi C, Gaetani M, Rebane A, Liiv I, Maran U, Mollica L, Bottomley MJ, Musco G, Peterson P (2008) The Autoimmune Regulator PHD finger binds non-methylated Histone H3K4 to activate gene expression. EMBO Reports 9, 370-6   Hetenyi C*, Maran U, Garcia-Sosa AT, Karelson M (2007) Structure-based calculation of drug efficiency indices. Bioinformatics 23, 2678-85   Hetenyi C*, van der Spoel D (2006) Blind docking of drug-sized compounds to proteins with up to a thousand residues. FEBS Letters 580, 1447-50   Hetenyi C*, Paragi G, Maran U, Timar Z, Karelson M, Penke B (2006) Combination of a modified scoring function with two-dimensional descriptors for calculation of binding affinities of bulky, flexible ligands to proteins. J Am Chem Soc 128, 1233-9   Fodor K, Harmat V, Hetenyi C, Kardos J, Antal J, Perczel A, Patthy A, Katona G, Graf L (2005) Extended intermolecular interactions in a serine protease-canonical inhibitor complex account for strong and highly specific inhibition. J Mol Biol 350, 156-69   Kovacs M, Toth J, Hetenyi C, Malnasi-Csizmadia A, Sellers JR (2004) Mechanism of blebbistatin inhibition of myosin II. J Biol Chem 279, 35557-63   Hetenyi C*, Szabo Z, Klement E, Datki Z, Kortvelyesi T, Zarandi M, Penke B (2002) Pentapeptide amides interfere with the aggregation of beta amyloid peptide of Alzheimer's disease. Biochem Biophys Res Comm, 292, 931-6   Hetenyi C, van der Spoel D (2002) Efficient docking of peptides to proteins without prior knowledge of the binding site. Protein Sci, 11, 1729-37   Hetenyi C*, Kortvelyesi T, Penke B (2002) Mapping of the possible binding sequences of two beta-sheet breaker peptides on beta amyloid peptide of Alzheimer's disease. Bioorgan Med Chem, 10, 1587-93

TEACHING MATERIAL (password protected pages)

Introduction to structural modeling of bioactive molecules

Calculation of molecular interactions

Protein science (in Hungarian, ELTE MSc course)

Professional activities
PhD supervisor of three PhD students
Lecturer of PhD and MSc courses in protein science, structural bioinformatics of drug design, calculation of molecular interactions, and medical chemistry
Member of doctoral committees, doctoral examiner, and doctoral opponent (several times)
Member of scientific societies: American Chemical Society (USA, -2013), The Protein Society (USA) Member of organizing committee of conference MedChem & CADD-2013 (Las Vegas, USA) Referee of scientific journals J Am Chem Soc, Proteins, Protein Sci, Expert Opin Drug Discov, J Comput Chem, J Comput-Aided Mol Design, J Chem Inf Model, Bioorgan Med Chem, Mini Rev Med Chem, Plos Comp Biol, Chem Phys Lett, Food and Chemical Toxicology Prizes 2013 Bolyai Diploma for outstanding research work in the period of 2009-2012 Bolyai Curatory, Hungarian Academy of Sciences 2011 Talentum Academy Award Central-European Talent Search Foundation, Hungarian Academy of Sciences, amount: 20 000 EUR 1999 Special prize for MSc Thesis Hungarian Chemical Society





Hungarian Academy of Sciences











Eötvös University







/////Csaba Hetenyi, Hungarian Academy of Sciences , Eötvös University

Khyati khanna

Assistant Manager- Intellectual Property Management

Dr. Reddy's Laboratories

LINKS

https://in.linkedin.com/pub/khyati-khanna/18/936/832

Khyati Khanna - Google+

https://plus.google.com/105519231838199643119

Khyati Khanna, Jubilant Lifesciences Ltd - India | Viadeo

in.viadeo.com/en/profile/khyati.khanna

https://www.facebook.com/khyati.khanna

  

 

Experience

Assistant Manager- Intellectual Property Management

Dr. Reddy's Laboratories

June 2015 – Present (5 months)

Research Scientist

Jubilant Generics ltd (formerly Jubilant lifesciences ltd)

July 2014 – July 2015 (1 year 1 month)Noida

Research Scientist

Hikal Ltd, Pune

February 2015 – May 2015 (4 months)

Research Associate

Jubilant Life Sciences Ltd

June 2011 – June 2014 (3 years 1 month)Noida Area, India

Analytical Chemist

Bureau Veritas Consumer Products Services

September 2010 – May 2011 (9 months)

Trainee

Jubilant Organosys Ltd

January 2010 – June 2010 (6 months)

done internship in jubilant organosys

Education

National Academy of Legal Studies and Research (NALSAR University Of Law)

Post Graduate Diploma in Patent Law, Intellectual Property Rights

2010 – 2011

Banasthali Vidyapith

M.Sc in Pharmaceutical Chemistry, Pharmaceutical Chemistry

2008 – 2010

Kurukshetra University

B.Sc, Industrial Microbiology

2005 – 2008

Modern Era Public School

Senior Secondary, Physics, Chemistry, Biology

WIPO

DL-101, Certificate Course On Basic of Intellectual Property Rights

National Academy of Legal Studies and Research (NALSAR University Of Law)

Shameerpet, Hyderabad, 

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Elizabeth Quijano

Elizabeth Quijano, ASQ CQA/CBA

Quality Compliance Professional/ Certified Quality/Biomedical Auditor (ASQ-CQA/CBA)/GMP Trainer/B.Sc. Biochemistry

https://ca.linkedin.com/in/elizabethquijano

• power_speaking
• ElizabethQuijan

 

E-mail: lizquijano@live.com
Tel: 416-843-0611

  

Summary

Process driven Quality compliance professional with 11 years demonstrated experience in GMP compliance strategy, set-up, and implementation related to the manufacturing, importation (MRA and non-MRA) and distribution of pharmaceuticals, biologics, medical devices and natural health products. Extensive knowledge in Current Good Manufacturing Practices (cGMP) for biologics, pharmaceuticals and natural health products, USFDA CFR 210-211, USFDA 820, ICH, Medical Device Regulation, ISO 13485 and ISO 9001, Good Distribution Practices, and Good Pharmacovigilance Practice (GVP).

Certification: Certified Quality Auditor (ASQ)
: Certified Biomedical Auditor (ASQ)
Education: B.Sc. Biochemistry
Specialties:
• Regulatory inspection
• Regulatory communication
• Establishment/Site Licensing
• GMP audit
• GMP training
• Product Release (i.e. BGTD Lot Release, Special Access Programme)
• Product Testing (i.e. Stability, Confirmatory, Identity)
• Quality Management System (i.e. Deviation, Corrective/Preventative Action (CAPA) and Out of Specification (OOS) Investigation, Change Control, Complaint and Adverse Reaction)
• Quality Agreements
• GMP Compliance (i.e. Validation, Annual Product Review, Batch Record Review, Alternate Sample Retention, Unique ID Certification)
• GMP records (i.e. Standard Operating Procedure, protocol, reports, checklist)
• Logistics GMP (i.e. Transportation Studies)
 

Liz Quijano

@ElizabethQuijan

Experience

Quality Compliance Professional, ASQ Certified

Compliance strategy, set-up, and implementation to pharmaceutical and medical device industry

2015 – Present (less than a year)Canada

Manage activities related to company's compliance to GMP or Medical Device Regulation. This will include GMP audit, Training, Change Control, CAPA, Complaint and Adverse Event, RECALL,
Annual compliance (i.e. Stability and Confirmatory testing, Annual Product Quality Review, Batch Record Review, Annual Validation Summary Reports) ,develop GMP records (i.e Quality Agreement, Standard Operating Procedures) and product release. Host regulatory inspections.
Continuously improve the overall quality system. Track quality assurance metrics for the organization. Manage relationship with vendors and regulatory authorities. Manage all activities specific to Establishment/Site Licensing.

Continuing Education Professor

Humber College

2011 – Present (4 years)Ontario, Canada

Course:
Communication Techniques for Quality Assurance (2011-2012)

Topics:
Business Correspondence
How to write SOP
How to write informational, analytical and recommendation report
How to write positive, negative and persuasive message
Listening skills
Team Dynamics
How to deliver presentation
How to provide feedback

Senior Quality Lead

Unilever

2013 – 2015 (2 years)Toronto, Ontario, Canada

Managed all activities related to Unilever’s compliance to all applicable Health Canada regulation for the importation and distribution of DIN and NHP products. Ensure foreign sites, warehouse and laboratories are in compliance to Canadian GMP. Managed all activities specific to Establishment/Site Licensing application/amendment and renewal of Unilever Canada, foreign sites and warehouse.

QA Consultant

PharmEng Technology

2012 – 2013 (1 year)Ontario, Canada

Provided consulting services to pharmaceuticals, biologics, natural health products, cosmetics, disinfectants, active pharmaceutical ingredients and medical devices companies.

Projects:
Quality Control Officer
GMP Audit
GMP Training
Annual Product Quality Review Preparation
Development of Standard Operating Procedure (SOP)

Instructor

Academy of Applied Pharmaceutical Sciences

2012 – 2012 (less than a year)Ontario, Canada

Course: Good Manufacturing Practices (Level I)

Complaints Specialist

Agfa Healthcare

2011 – 2012 (1 year)Waterloo Ontario Canada

Reviewed complaints for appropriateness of root cause analysis, completion and effectiveness of Corrective and Preventative Action (CAPA) and compliance to all applicable regulations and current procedures.

QA Manager

Summit Veterinary Pharmacy Inc.

2010 – 2011 (1 year)Toronto, Ontario, Canada

Set up and implemented Quality Management Program

Quality Specialist

Baxter Healthcare

2006 – 2010 (4 years)Toronto, Ontario, Canada

Managed all activities related to product release and compliance of biologics, drug imports (MRA and non-MRA), medical devices, clinical trial products and Special Access Programme (SAP) products to GMP, Medical Device Regulations and Baxter Quality Management System. Oversee UPS-SCS compliance to GMP, Medical Device Regulations and Baxter Quality Management System.

QA Manager

Pax-All Manufacturing Inc.

2004 – 2006 (2 years)Toronto, Ontario, Canada

Managed all activities (i.e. release, development of specifications, deviation and CAPA, complaints, supplier non-conformances, in process testing, batch record review) related to Pax-All’s compliance to ISO 9001, Health Canada Good Manufacturing Practices and customer requirements for the manufacture of Category IV monograph and Natural Health Products.

Laboratory Technician

Pax-All Manufacturing Inc.

2003 – 2004 (1 year)Missssauga, Ontario, Canada

Provided support to the Quality Assurance Manager on the development of Quality Management System that met Health Canada and ISO 9001 certification.

Education

University of Santo Tomas

B.Sc., Biochemistry

1992 – 1996

Humber College

Quality Management Program

Course Taken:
Quality Concepts
Quality Auditing
Six Sigma

Seneca College of Applied Arts and Technology

Certificate, Regulatory Affairs and Quality Operations

Course Taken:
Pharmaceutical Manufacturing and Formulation
Regulatory Affairs Level I and II

Volunteer Experience & Causes

Workshop Provider

American Society for Quality (ASQ)

November 2012Education

Title: Effective Business Correspondence

Scope:
This course focused on one of the most basic type of communication that happens in the workplace, business correspondence. In this course, participants learned the different types of correspondence common in the workplace and their uses, the process in writing correspondence, how to write correspondence that will obtain the maximum audience...more

 

Workshop Provider

American Society For Quality (ASQ)

May 2013Science and Technology

Seminar: Handling Regulatory Inspection In The Pharmaceutical Industry

Scope:
This interactive seminar focused on strategies for handling regulatory inspection in the pharmaceutical indsutry . In this seminar, participants got an overview of the audit process, how to prepare their facility and personnel for an audit, audit do’s and don’ts, and how to respond to audit questions.
This...more

Designation: Competent Communicator (CC), Advanced Leader Bronze (ALB)

Toastmasters International

2011 – Present (4 years)Education

o President, U-Toast Club, 2014-2015
o Vice President Education, U-Toast Club, 2013-2014
o President, Power Speaking Club, 2013
o Vice President, Public Relations, 2012
o Club International Speech Contest (1st Place), 2013
o Club Humorous Contest (1st Place), 2012
o Event Speaker at District 86 Speakers Bureau, 2012-2013

Honors & Awards

ISO 13485:2003 Lead Auditor (TPECS)

BSI

August 2015

Certification # 8282933-142427

Additional Honors & Awards

ASQ CQA (Certified Quality Auditor)
ASQ CBA (Certified Biomedical Auditor)

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