2pm Utc To Cet

2pm

Converting CST to CET. This time zone converter lets you visually and very quickly convert CST to CET and vice-versa. Simply mouse over the colored hour-tiles and glance at the hours selected by the column. CST stands for Central Standard Time. CET is known as Central European Time. CET is 7 hours ahead of CST. Time Difference. Central European Summer Time is 2 hours ahead of Universal Time Coordinated 4:30 am 04:30 in CEST is 2:30 am 02:30 in UTC. CET to UTC call time Best time for a conference call or a meeting is between 9am-6pm in CET which corresponds to 8am-5pm in UTC. Observes CET – Central European Time part of the year, but not currently. Currently has same time zone offset as CET (UTC +1) but different time zone name. Central European Time (CET) is 1 hour ahead of Coordinated Universal Time (UTC). This time zone is in use during standard time in: Europe, Africa.

DAY 1 – FEBRUARY 16, 2021


Streamlined, step-by-step process development for clinical and commercial manufacturing of cell therapies
9am EST / 2pm GMT / 3pm CET

Dr. Behnam Ahmadian Baghbaderani will be highlighting the current challenges associated with industrialization of cell therapies and explain how Lonza is addressing these challenges. In particular, he will be focusing on some of the best practices of process development and analytical method development with emphasis on a streamlined, phase appropriate, step by step development approach for cell and gene therapies established at Lonza. He is going to explain what would be the benefits of appropriate process development activities and partnering to de-risk the manufacturing of cell therapies and pave the way for future commercialization.

Speakers:

TAI, Temps Atomique International, is theinternational atomic time scale based on a continuous countingof the SI second. TAI is currently ahead of UTC byTAI is always ahead of GPS by 19 seconds. See also: Nixie Tube Leap Second Countdown Clock. Pacific DAYLIGHT Time. P D T (UTC- 7) 07:45:32 P.M. Mountain DAYLIGHT Time. M D T (UTC- 6) 08:45:32 P.M. How to get current time-stamp in UTC/GMT and then How to convert this time-stamp into seconds? Itry this but its thrw exception. SimpleDateFormat sdfu = new SimpleDateFormat ('yyyy-MM-dd kk:mm'); Date udate = sdfu.parse (dateAndTimeUTC); long timeInMillisSinceEpoch123 = udate.getTime ; long durationinSeconds2 = timeInMillisSinceEpoch123 / 1000; System.out.println ('Time in Seconds UTC: '. The Current Epoch Unix Timestamp. Seconds since Jan 01 1970. Current utc time with seconds calculator.

  • UTC to EST Time Converter. Convert UTC time to Eastern Standard Time (North America).EST time zone offset is UTC-05.
  • UTC to CET call time Best time for a conference call or a meeting is between 8am-5pm in UTC which corresponds to 9am-6pm in CET 2:00 pm Universal Time Coordinated (UTC).

Behnam Ahmadian Baghbaderani
Global Head of Process Development, Cell & Gene Technologies
Lonza

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Process Development Considerations & Strategies
10am EST / 3pm GMT / 4pm CET

Session Description is Coming Soon!

2pm cet time

Speaker:

Anne- Sophie Lebrun
Head of Operations
Bone Therapeutics, Belgium

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DAY 2 – FEBRUARY 17, 2021


Beyond Conventional LBAs: Accelerating Viral Vector Bioanalysis Using Microfluidic Immunoassays with Nanoliter Sample Volumes and Results in One-Hour
9am EST / 2pm GMT / 3pm CET

Viral vector quantification using conventional immunoassays suffers from narrow dynamic ranges, large sample volumes, and laborious procedures. In this webcast, we present data on the high-precision, automated microfluidic immunoassays for the quantification of AAV and lentiviral vectors in bioprocessing applications. Examples of the rapid implementation of AAV titer assays are presented for multiple AAV serotypes.

Speaker:

Rob Durham, PhD
Director of Service and Scientific Support
Gyros Protein Technologies

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A Cell Therapy Media Fill Protocol for Validation of Aseptic Processing of Cord Blood
10am EST / 3pm GMT / 4pm CET

We present the design of a media fill study protocol using sterile growth medium in place of cord blood for validation of aseptic processing. Growth media are pre-qualified for ability to support growth of relevant microorganisms as visualized in media turbidity assays. Annual completion of media fills are required for all active processing staff to verify use of proper aseptic techniques, executed under ‘worst-case’ conditions stressing the system. Dynamic environmental and personnel monitoring is included to detect actual contamination risks during the media fills. After processing, all simulated products and controls are incubated and examined for media turbidity. The acceptable failure rate (i.e. observation of turbidity) is defined as zero (0%). This media fill program was approved by FDA to support the manufacture of HPC, Cord Blood under license. As such, our experience can provide insight into the regulatory expectations for media fill protocols for growing assortments of cellular therapeutics under development towards regulatory approval in the industry.

Speaker:

Wouter Van’t Hof
Director, Processing Facility & CEO
Cell Therapy Incubator, Cleveland Cord Blood Center, USA [email protected]

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DAY 3 – FEBRUARY 18, 2021


Commercial Ready Analytical Platforms for T-cell Therapies
9am EST / 2pm GMT / 3pm CET

Dr. Jef Pinxteren, Director of Process and Analytical Development at Catalent Cell and Gene Therapy, will discuss a breadth of analytical methodologies facilitating manufacturing design and accelerating CAR-T therapies to commercial readiness phase.

  • Attendees will be able to gain insight into:
  • Benefits of working with a full-service provider of analytical methods
  • Strategy and process flow from analytical assay development to GMP implementation for clinical and commercial manufacturing
  • Emerging strategies for cell therapy product identification, characterization and potency testing using state-of-the-art technologies
  • Definition of framework for analytical method validation ensuring fast batch release

Speaker:

Dr. Jef Pinxteren
Director of Process and Analytical Development
Catalent Cell and Gene Therapy

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Detection of replication competent viruses in viral vector products
10am EST / 3pm GMT / 4pm CET

Session Description is Coming Soon!

Speaker:

Matthew Pennington, PhD
Scientist 1
Biologics Testing Solutions, Charles River Laboratories

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Cell Therapy Analytics – Analytical Method Development & Validation
11am EST / 4pm GMT / 5pm CET

2pm Utc To Cet

Advanced therapy medicinal product (ATMP) characterization and analysis play an important role in providing CMC information and supporting release and stability studies. Cell and patient variability, multiple MOAs, lack of reference materials and complex analytical methods and instruments underlie some of the difficulties of developing analytical methods. The presentation will present different assays for characterization, potency, purity and identity testing and will follow different analytical challenges, from the development stage up to validation, including case studies.

Speaker:

Ruti Goldberg
Compliance & Methods Validation Manager
Pluristem Therapeutics Inc., Israel

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2pm cet to cst

DAY 4 – FEBRUARY 19, 2021


ELEVECTA® - Helper virus-free AAV production with stable CAP® and HEK293 producer cells
9am EST / 2pm GMT / 3pm CET

Learn in this webinar how to:

  • Close the production gap for AAV gene therapy vectors by using ELEVECTA® stable helper virus-free AAV producer cell lines
  • Eliminate any transient transfection step from your AAV production process
  • Achieve reliable AAV production by simple induction of suspension producer cells
  • Optimize scale-up production of AAV in stirred tank bioreactors

Speaker:

Dr. Silke Wissing
Chief Scientific Officer
CEVEC Pharmaceuticals GmbH

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CMC Considerations for NK Cell Therapy
10am EST / 3pm GMT / 4pm CET

NK cells have become to new focus point of the cell therapy industry. Kiadis Pharma is developing an off the shelf NK cell therapy platform for multiple indications in oncology and infectious disease. Development of such a platform and the potential to scale this to biologics industrial scale require a solid CMC strategy already in early phase. This talk will provide an overview of the most important CMC considerations which should be addressed from the start. Specifically for:

  • Starting materials
  • Expansion process: towards a homogeneous cell suspension
  • Analytical panel: flow assays, biochemical assays, cell-based assays
  • Filling and Freezing

Speakers:

2pm Utc To Cet

Utc Conversion To Cet

Mathieu Streefland
Vice President CMC Development
Kiadis, The Netherlands

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2 Pm Utc To Cest

Convert timezones and find the best time for your meeting in (GMT-12:00) International Date Line West, (GMT-11:00) American Samoa, (GMT-11:00) Midway Island, (GMT-10:00) Hawaii, (GMT-09:00) Alaska, (GMT-08:00) Pacific Time (US & Canada), (GMT-08:00) Tijuana, (GMT-07:00) Arizona, (GMT-07:00) Chihuahua, (GMT-07:00) Mazatlan, (GMT-07:00) Mountain Time (US & Canada), (GMT-06:00) Central America, (GMT-06:00) Central Time (US & Canada), (GMT-06:00) Guadalajara, (GMT-06:00) Mexico City, (GMT-06:00) Monterrey, (GMT-06:00) Saskatchewan, (GMT-05:00) Bogota, (GMT-05:00) Eastern Time (US & Canada), (GMT-05:00) Indiana (East), (GMT-05:00) Lima, (GMT-05:00) Quito, (GMT-04:00) Atlantic Time (Canada), (GMT-04:00) Caracas, (GMT-04:00) Georgetown, (GMT-04:00) La Paz, (GMT-04:00) Puerto Rico, (GMT-04:00) Santiago, (GMT-03:30) Newfoundland, (GMT-03:00) Brasilia, (GMT-03:00) Buenos Aires, (GMT-03:00) Greenland, (GMT-03:00) Montevideo, (GMT-02:00) Mid-Atlantic, (GMT-01:00) Azores, (GMT-01:00) Cape Verde Is., (GMT+00:00) Edinburgh, (GMT+00:00) Lisbon, (GMT+00:00) London, (GMT+00:00) Monrovia, (GMT+00:00) UTC, (GMT+01:00) Amsterdam, (GMT+01:00) Belgrade, (GMT+01:00) Berlin, (GMT+01:00) Bern, (GMT+01:00) Bratislava, (GMT+01:00) Brussels, (GMT+01:00) Budapest, (GMT+01:00) Casablanca, (GMT+01:00) Copenhagen, (GMT+01:00) Dublin, (GMT+01:00) Ljubljana, (GMT+01:00) Madrid, (GMT+01:00) Paris, (GMT+01:00) Prague, (GMT+01:00) Rome, (GMT+01:00) Sarajevo, (GMT+01:00) Skopje, (GMT+01:00) Stockholm, (GMT+01:00) Vienna, (GMT+01:00) Warsaw, (GMT+01:00) West Central Africa, (GMT+01:00) Zagreb, (GMT+01:00) Zurich, (GMT+02:00) Athens, (GMT+02:00) Bucharest, (GMT+02:00) Cairo, (GMT+02:00) Harare, (GMT+02:00) Helsinki, (GMT+02:00) Jerusalem, (GMT+02:00) Kaliningrad, (GMT+02:00) Kyiv, (GMT+02:00) Pretoria, (GMT+02:00) Riga, (GMT+02:00) Sofia, (GMT+02:00) Tallinn, (GMT+02:00) Vilnius, (GMT+03:00) Baghdad, (GMT+03:00) Istanbul, (GMT+03:00) Kuwait, (GMT+03:00) Minsk, (GMT+03:00) Moscow, (GMT+03:00) Nairobi, (GMT+03:00) Riyadh, (GMT+03:00) St. Petersburg, (GMT+03:00) Volgograd, (GMT+03:30) Tehran, (GMT+04:00) Abu Dhabi, (GMT+04:00) Baku, (GMT+04:00) Muscat, (GMT+04:00) Samara, (GMT+04:00) Tbilisi, (GMT+04:00) Yerevan, (GMT+04:30) Kabul, (GMT+05:00) Ekaterinburg, (GMT+05:00) Islamabad, (GMT+05:00) Karachi, (GMT+05:00) Tashkent, (GMT+05:30) Chennai, (GMT+05:30) Kolkata, (GMT+05:30) Mumbai, (GMT+05:30) New Delhi, (GMT+05:30) Sri Jayawardenepura, (GMT+05:45) Kathmandu, (GMT+06:00) Almaty, (GMT+06:00) Astana, (GMT+06:00) Dhaka, (GMT+06:00) Urumqi, (GMT+06:30) Rangoon, (GMT+07:00) Bangkok, (GMT+07:00) Hanoi, (GMT+07:00) Jakarta, (GMT+07:00) Krasnoyarsk, (GMT+07:00) Novosibirsk, (GMT+08:00) Beijing, (GMT+08:00) Chongqing, (GMT+08:00) Hong Kong, (GMT+08:00) Irkutsk, (GMT+08:00) Kuala Lumpur, (GMT+08:00) Perth, (GMT+08:00) Singapore, (GMT+08:00) Taipei, (GMT+08:00) Ulaanbaatar, (GMT+09:00) Osaka, (GMT+09:00) Sapporo, (GMT+09:00) Seoul, (GMT+09:00) Tokyo, (GMT+09:00) Yakutsk, (GMT+09:30) Adelaide, (GMT+09:30) Darwin, (GMT+10:00) Brisbane, (GMT+10:00) Canberra, (GMT+10:00) Guam, (GMT+10:00) Hobart, (GMT+10:00) Melbourne, (GMT+10:00) Port Moresby, (GMT+10:00) Sydney, (GMT+10:00) Vladivostok, (GMT+11:00) Magadan, (GMT+11:00) New Caledonia, (GMT+11:00) Solomon Is., (GMT+11:00) Srednekolymsk, (GMT+12:00) Auckland, (GMT+12:00) Fiji, (GMT+12:00) Kamchatka, (GMT+12:00) Marshall Is., (GMT+12:00) Wellington, (GMT+12:45) Chatham Is., (GMT+13:00) Nuku'alofa, (GMT+13:00) Samoa, and (GMT+13:00) Tokelau Is.