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Comments

Gail Meyers

5 years ago from Kansas City - United States

This is one I don't think I've ever tried. Thanks for the informative and interesting hub. Voted up, useful and shared.

AUTHOR

Dolores Monet

5 years ago from East Coast, United States

Maren Morgan - actually, a lot of houseplants are toxic. I used to buy poinsettias for Christmas, and even got one to rebloom beautifully, but now with a cat, I must be so careful. Well, you can't have everything!

Jamie Brock - Swiss Cheese plants were popular in the 1970s, a big time for houseplants. They used to grow Monstera deliciosa on these big hunks of bark. But the leaves were not so huge. When you see plants in malls and public places, that usually means they are easy to grow and maintain! Thanks!

DDE - thanks!

Devika Primić

5 years ago from Dubrovnik, Croatia

Most interesting, I had no idea of such a unique plant, thanks for the well researched hub.

Jamie Brock

5 years ago from Texas

Thank you for this informative hub about the Swiss Cheese Plant. I see these plants in large planters in malls and inside other places and I think they are just gorgeous! As pretty as they are and as big as they get, I figured they would be a tough one to grow but they seem fairly easy to take care of from what you have written. I may have to get one or even a couple. What a wonderful, informative hub, thanks for sharing!

Maren Elizabeth Morgan

5 years ago from Pennsylvania

Rats!! I was already to start looking for one until you mentioned "toxic to cats." Still a great article!

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4. Saxofón.

5. Batería. De acuerdo con el experto Barry Bittman, la práctica constante de éste estimula el sistema inmunológico, con lo que se puede evitar enfermedades como lagripe. Además de revertir los daños producidos por elestrés cotidiano.

5. Batería.

Las actividades sincronizadas, como la música o la danza fomentan sentimientos de conexión social, confianza interpersonal y vinculación. Muchas actividades humanas y animales son rítmicas: caminar, hablar, aplaudir y bailar” afirma Mona Lisa Chanda y Daniel Levitin, expertos del departamento de Sicología de la Universidad McGill de Montreal en Canadá.

Universidad McGill de Montreal en Canadá.

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Note: For ACTs studying a device product not previously approved or cleared by FDA for any use and that are required to be registered, full posting of the clinical trial information on ClinicalTrials.gov ordinarily is delayed until after the device product has been approved or cleared. See the Device Product Not Approved or Cleared by U.S. FDA data element on ClinicalTrials.gov. The Final Rule states that the responsible party may authorize the National Institutes of Health (NIH) to publicly post clinical trial registration information for an applicable device clinical trial of a device product that has not been previously approved or cleared by the U.S. FDA.

For complete statutory definitions and more information on the meaning of Applicable Clinical Trial, see the Checklist and Elaboration for Evaluating Whether a Clinical Trial or Study is an Applicable Clinical Trial (ACT) ("ACT Checklist"), which follow the criteria specified in 42 CFR 11.22(b), to determine whether a study initiated on or after January 18, 2017, is an ACT subject to the expanded registration requirements under the Final Rule. Although the ACT Checklist and Elaboration document is intended for use with respect to determining the requirements for clinical trials or studies initiated on or after January 18, 2017, it may also be useful in evaluating whether a clinical trial or study that was initiated before January 18, 2017, is an ACT, even though such trials or studies are not subject to the expanded registration requirements in the Final Rule.

before

For more information, see the following frequently asked questions (FAQs):

Regulations (42 CFR Part 11)

Overall, the final rule clarifies which clinical trials of FDA-regulated drug products (including biological products) and device products and which pediatric postmarket surveillances of a device product, are applicable clinical trials for which information must be submitted to ClinicalTrials.gov. The final rule considers all clinical trials with one or more arms and with one or more pre-specified outcome measures to be controlled clinical trials. The final rule explains that we have determined that no expanded access use would be considered an applicable clinical trial under section 402(j) of the PHS Act. The final rule also describes an approach for evaluating, prior to registration, whether a particular clinical trial or study is an applicable clinical trial. [81 FR 64982] For more information on regulatory requirements, see 42 CFR Part 11 . For additional information on evaluating whether a study is an applicable clinical trial, see the Checklist and Elaboration for Evaluating Whether a Clinical Trial or Study is an Applicable Clinical Trial (ACT) (PDF).

Key regulatory provisions and related discussions in the Final Rule (81 FR 64981) include:

Pediatric postmarket surveillances of device products ordered under Section 522 of the FDC Act (PDF) as amended by Section 307 of FDAAA are considered ACTs and must be registered on ClinicalTrials.gov and have results information submitted.

We'll help you find the answer or connect with an advisor.

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