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Meet With Us in 2022

October 22-26, 2022 –  American Society of Reproductive Medicine (ASRM) – Anaheim, CA https://www.asrm.org/events/upcoming-meetings/events/2022-10-22/

March 23-27, 2022 – Pacific Coast Reproductive Society – Rennaissance Esmeralda Resort & Spa, India Wells, CA – https://www.pcrsonline.org/annual-meeting

October 17-20, 2021 – American Society of Reproductive Medicine (ASRM) – Baltimore, MD https://www.asrm.org/events/upcoming-meetings/events/2021-10-16/

September 14-15, 2021 – Women’s Health Innovation Summit – Boston, MA https://womenshealthinnovationusa.com/events/womens-health-innovation-summit-2021

March 25-29, 2020 – Pacific Coast Reproductive society –  Renaissance Esmeralda Resort & Spa, Indian Wells, CA – https://www.pcrsonline.org/2020-annual-meeting

May 1 – 2, 2020 – New England Fertility Society – Gurney’s Hotel, Newport, RI –https://www.nefs.org/2020annualmeeting.htm

June 3 – 6, 2020 – Midwest Reproductive Symposium International – Chicago, IL – http://www.midwestreproductivesymposium.com

October 17 – 21, 2020 – American Society of Reproductive Medicine (ASRM)- Portland, OR – https://www.asrm.org/events/upcoming-meetings/events/2020-10-17/

Apr 23, 2018 Focus On Fertility Talks ReceptivaDx

Oct 15, 2018 ReceptivaDx at the ASRM Expo

Campaigns

March 31, 2022 – Women’s Health Campaign with Media Planet USA Future of Personal Health

December 28, 2021 – Future of Fertility/Family at Home Campaign with Media Planet USA An Expert Explains Endometriosis

October 23, 2021 – Fertility Rally

September 2021 – Maternal Health Campaign with Media Planet USA – When Contemplating IVF, Educate and Advocate

March 2021 – Future of Fertility Campaign with Media Planet USA – Future of Fertility

The ReceptivaDxTM Test was developed by Cicero Diagnostics in conjunction with Pathology Consultants, Inc. of Greenville, SC. Pathology Consultants, Inc. is a laboratory certified under the Clinical Laboratory Improvement Amendments (CLIA). As with other laboratory-developed tests, this testing service has not been cleared or approved by the US FDA or any other federal regulatory agencies. Data have not been submitted to or evaluated by Federal regulatory agencies and the test is not for sale as an In Vitro Diagnostic (IVD) in the US or the EU.


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